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'en:chylomicron retention disease'
(id=6819005 ; fe=en:chylomicron retention disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=32259 creation date=2017-06-25 touchdate=2025-07-27 23:35:47.000)
≈ 573 relations sortantes

  1. en:chylomicron retention disease -- r_associated #0: 49 / 1 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:chylomicron retention disease | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=49
  2. en:chylomicron retention disease -- r_associated #0: 47 / 0.959 -> en:baller-gerold syndrome
    n1=en:chylomicron retention disease | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=47
  3. en:chylomicron retention disease -- r_associated #0: 47 / 0.959 -> en:northern epilepsy syndrome
    n1=en:chylomicron retention disease | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=47
  4. en:chylomicron retention disease -- r_associated #0: 46 / 0.939 -> en:basal ganglia disease, biotin-responsive
    n1=en:chylomicron retention disease | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=46
  5. en:chylomicron retention disease -- r_associated #0: 46 / 0.939 -> en:glycogen storage disease type i
    n1=en:chylomicron retention disease | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=46
  6. en:chylomicron retention disease -- r_associated #0: 46 / 0.939 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:chylomicron retention disease | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=46
  7. en:chylomicron retention disease -- r_associated #0: 46 / 0.939 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:chylomicron retention disease | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=46
  8. en:chylomicron retention disease -- r_associated #0: 45 / 0.918 -> en:morquio syndrome
    n1=en:chylomicron retention disease | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=45
  9. en:chylomicron retention disease -- r_associated #0: 45 / 0.918 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:chylomicron retention disease | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=45
  10. en:chylomicron retention disease -- r_associated #0: 45 / 0.918 -> en:type ii acrocephalopolysyndactyly
    n1=en:chylomicron retention disease | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=45
  11. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:acid phosphatase deficiency
    n1=en:chylomicron retention disease | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=44
  12. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:acrodermatitis enteropathica
    n1=en:chylomicron retention disease | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=44
  13. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:chylomicron retention disease | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=44
  14. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:fronto-facio-nasal dysplasia
    n1=en:chylomicron retention disease | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=44
  15. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:gracile syndrome (disorder)
    n1=en:chylomicron retention disease | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=44
  16. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:hyperphosphatasia with mental retardation
    n1=en:chylomicron retention disease | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=44
  17. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:chylomicron retention disease | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=44
  18. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:reardon hall slaney syndrome
    n1=en:chylomicron retention disease | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=44
  19. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:rna polymerase iii-related leukodystrophy
    n1=en:chylomicron retention disease | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=44
  20. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:sar1b, 4-bp dup, 555ttac
    n1=en:chylomicron retention disease | n2=en:sar1b, 4-bp dup, 555ttac | rel=r_associated | relid=0 | w=44
  21. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:tungland bellman syndrome
    n1=en:chylomicron retention disease | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=44
  22. en:chylomicron retention disease -- r_associated #0: 44 / 0.898 -> en:walker-warburg syndrome
    n1=en:chylomicron retention disease | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=44
  23. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:chylomicron retention disease | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=43
  24. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:chylomicron retention disease | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=43
  25. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:ethanolaminosis
    n1=en:chylomicron retention disease | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=43
  26. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:hereditary factor xi deficiency disease
    n1=en:chylomicron retention disease | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=43
  27. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:hmg-coa lyase deficiency
    n1=en:chylomicron retention disease | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=43
  28. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:chylomicron retention disease | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=43
  29. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:marles greenberg persaud syndrome
    n1=en:chylomicron retention disease | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=43
  30. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:n-acetylglutamate synthase deficiency
    n1=en:chylomicron retention disease | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=43
  31. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:chylomicron retention disease | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=43
  32. en:chylomicron retention disease -- r_associated #0: 43 / 0.878 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:chylomicron retention disease | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=43
  33. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> Anderson
    n1=en:chylomicron retention disease | n2=Anderson | rel=r_associated | relid=0 | w=42
  34. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:chylomicron retention disease | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=42
  35. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:alkaptonuria
    n1=en:chylomicron retention disease | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=42
  36. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:aminomethyltransferase deficiency
    n1=en:chylomicron retention disease | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=42
  37. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:chylomicron retention disease | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=42
  38. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:chylomicron retention disease | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=42
  39. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:autosomal recessive scid
    n1=en:chylomicron retention disease | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=42
  40. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:becker generalized myotonia
    n1=en:chylomicron retention disease | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=42
  41. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:brachydactyly syndrome type b
    n1=en:chylomicron retention disease | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=42
  42. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:chylomicron retention disease | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=42
  43. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:congenital adrenal hyperplasia
    n1=en:chylomicron retention disease | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=42
  44. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:chylomicron retention disease | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=42
  45. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:cryptophthalmos syndrome
    n1=en:chylomicron retention disease | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=42
  46. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:cystinosis
    n1=en:chylomicron retention disease | n2=en:cystinosis | rel=r_associated | relid=0 | w=42
  47. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:deafness, progressive, with stapes fixation
    n1=en:chylomicron retention disease | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=42
  48. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=42
  49. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:infantile globoid cell leukodystrophy
    n1=en:chylomicron retention disease | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=42
  50. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:isovaleric acidemia
    n1=en:chylomicron retention disease | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=42
  51. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:kuskokwim disease
    n1=en:chylomicron retention disease | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=42
  52. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:lactase deficiency, congenital
    n1=en:chylomicron retention disease | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=42
  53. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:lethal congenital contracture syndrome 1
    n1=en:chylomicron retention disease | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=42
  54. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:macular corneal dystrophy
    n1=en:chylomicron retention disease | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=42
  55. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:microcephaly, amish type (disorder)
    n1=en:chylomicron retention disease | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=42
  56. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:mucopolysaccharidosis type i
    n1=en:chylomicron retention disease | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=42
  57. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:chylomicron retention disease | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=42
  58. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:pediatric failure to thrive
    n1=en:chylomicron retention disease | n2=en:pediatric failure to thrive | rel=r_associated | relid=0 | w=42
  59. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:peripheral nervous system disorder
    n1=en:chylomicron retention disease | n2=en:peripheral nervous system disorder | rel=r_associated | relid=0 | w=42
  60. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:pontocerebellar hypoplasia type 2
    n1=en:chylomicron retention disease | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=42
  61. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:pseudotrisomy 13 syndrome
    n1=en:chylomicron retention disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  62. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:pyruvate carboxylase deficiency
    n1=en:chylomicron retention disease | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=42
  63. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:reduced tendon reflexes
    n1=en:chylomicron retention disease | n2=en:reduced tendon reflexes | rel=r_associated | relid=0 | w=42
  64. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:retinitis punctata albescens (disorder)
    n1=en:chylomicron retention disease | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=42
  65. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:sanfilippo syndrome
    n1=en:chylomicron retention disease | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=42
  66. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:sar1b, glu122ter
    n1=en:chylomicron retention disease | n2=en:sar1b, glu122ter | rel=r_associated | relid=0 | w=42
  67. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:sar1b, gly37arg
    n1=en:chylomicron retention disease | n2=en:sar1b, gly37arg | rel=r_associated | relid=0 | w=42
  68. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:serum triglycerides normal
    n1=en:chylomicron retention disease | n2=en:serum triglycerides normal | rel=r_associated | relid=0 | w=42
  69. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> en:sitosterolemia with xanthomatosis
    n1=en:chylomicron retention disease | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=42
  70. en:chylomicron retention disease -- r_associated #0: 42 / 0.857 -> hyperglycéridémie mixte
    n1=en:chylomicron retention disease | n2=hyperglycéridémie mixte | rel=r_associated | relid=0 | w=42
  71. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:chylomicron retention disease | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=41
  72. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:alpha-1 antitrypsin deficiency
    n1=en:chylomicron retention disease | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=41
  73. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:alstrom syndrome
    n1=en:chylomicron retention disease | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=41
  74. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:arterial tortuosity syndrome
    n1=en:chylomicron retention disease | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=41
  75. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:atrophoderma vermiculatum
    n1=en:chylomicron retention disease | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=41
  76. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:chylomicron retention disease | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=41
  77. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:autosomal recessive inheritance
    n1=en:chylomicron retention disease | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=41
  78. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:chylomicron retention disease | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=41
  79. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:chylomicron retention disease | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=41
  80. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:congenital bowing of long bone
    n1=en:chylomicron retention disease | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=41
  81. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:congenital disorder of glycosylation type ia
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=41
  82. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:congenital pancreatic enterokinase deficiency
    n1=en:chylomicron retention disease | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=41
  83. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:congenital transferrin deficiency
    n1=en:chylomicron retention disease | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=41
  84. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:cystathionine beta-synthase deficiency disease
    n1=en:chylomicron retention disease | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=41
  85. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:familial renal iminoglycinuria
    n1=en:chylomicron retention disease | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=41
  86. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:glutamate-cysteine ligase deficiency
    n1=en:chylomicron retention disease | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=41
  87. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:gurrieri sammito bellussi syndrome
    n1=en:chylomicron retention disease | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=41
  88. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:chylomicron retention disease | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=41
  89. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:chylomicron retention disease | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=41
  90. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:hnsha due to glutathione reductase deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=41
  91. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:infantile hypophosphatasia
    n1=en:chylomicron retention disease | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=41
  92. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:jervell and lange nielsen syndrome
    n1=en:chylomicron retention disease | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=41
  93. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:joubert syndrome
    n1=en:chylomicron retention disease | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=41
  94. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:lipoidosis
    n1=en:chylomicron retention disease | n2=en:lipoidosis | rel=r_associated | relid=0 | w=41
  95. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:macdermot winter syndrome
    n1=en:chylomicron retention disease | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=41
  96. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:chylomicron retention disease | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=41
  97. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:microcephaly-capillary malformation syndrome
    n1=en:chylomicron retention disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  98. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:chylomicron retention disease | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=41
  99. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:neuraminidase deficiency
    n1=en:chylomicron retention disease | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=41
  100. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:neutral lipid storage disease with myopathy
    n1=en:chylomicron retention disease | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=41
  101. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:pelizaeus merzbacher like disease
    n1=en:chylomicron retention disease | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=41
  102. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:porphobilinogen synthase deficiency
    n1=en:chylomicron retention disease | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=41
  103. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:chylomicron retention disease | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=41
  104. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:severe diarrhea
    n1=en:chylomicron retention disease | n2=en:severe diarrhea | rel=r_associated | relid=0 | w=41
  105. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:chylomicron retention disease | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=41
  106. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> en:zellweger syndrome
    n1=en:chylomicron retention disease | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=41
  107. en:chylomicron retention disease -- r_associated #0: 41 / 0.837 -> rétention placentaire
    n1=en:chylomicron retention disease | n2=rétention placentaire | rel=r_associated | relid=0 | w=41
  108. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:2-hydroxyglutaric aciduria
    n1=en:chylomicron retention disease | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=40
  109. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:21-hydroxylase deficiency
    n1=en:chylomicron retention disease | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=40
  110. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:3-methylglutaconic aciduria type 3
    n1=en:chylomicron retention disease | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=40
  111. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:3-methylglutaconic aciduria type iv
    n1=en:chylomicron retention disease | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=40
  112. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:chylomicron retention disease | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=40
  113. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:adrenal gland hyperplasia ii
    n1=en:chylomicron retention disease | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=40
  114. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:chylomicron retention disease | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=40
  115. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:argininosuccinic aciduria
    n1=en:chylomicron retention disease | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=40
  116. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:aspartylglycosaminuria
    n1=en:chylomicron retention disease | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=40
  117. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:chylomicron retention disease | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=40
  118. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:autosomal recessive ocular albinism
    n1=en:chylomicron retention disease | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=40
  119. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:bardet-biedl syndrome
    n1=en:chylomicron retention disease | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=40
  120. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:behrens baumann dust syndrome
    n1=en:chylomicron retention disease | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=40
  121. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:chylomicron retention disease | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=40
  122. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:childhood hypophosphatasia (disorder)
    n1=en:chylomicron retention disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  123. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:chitty hall baraitser syndrome
    n1=en:chylomicron retention disease | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=40
  124. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:chylomicron retention disease | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=40
  125. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:congenital disorder of glycosylation type ic
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=40
  126. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:congenital dyserythropoietic anemia, type i
    n1=en:chylomicron retention disease | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=40
  127. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:congenital sucrase-isomaltase deficiency
    n1=en:chylomicron retention disease | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=40
  128. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:craniodiaphyseal dysplasia
    n1=en:chylomicron retention disease | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=40
  129. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:defect in chylomicron secretion
    n1=en:chylomicron retention disease | n2=en:defect in chylomicron secretion | rel=r_associated | relid=0 | w=40
  130. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:dicarboxylicaminoaciduria
    n1=en:chylomicron retention disease | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=40
  131. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:dubin-johnson syndrome
    n1=en:chylomicron retention disease | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=40
  132. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:fabry disease
    n1=en:chylomicron retention disease | n2=en:fabry disease | rel=r_associated | relid=0 | w=40
  133. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:factor v and factor viii, combined deficiency of
    n1=en:chylomicron retention disease | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=40
  134. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:chylomicron retention disease | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40
  135. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:chylomicron retention disease | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=40
  136. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:geroderma osteodysplastica
    n1=en:chylomicron retention disease | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=40
  137. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:glutathione synthetase deficiency
    n1=en:chylomicron retention disease | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=40
  138. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:hereditary factor xii deficiency disease
    n1=en:chylomicron retention disease | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=40
  139. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=40
  140. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:hyperimmunoglobulin e syndrome
    n1=en:chylomicron retention disease | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=40
  141. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:chylomicron retention disease | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=40
  142. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:jejunal endoscopy shows white epithelium
    n1=en:chylomicron retention disease | n2=en:jejunal endoscopy shows white epithelium | rel=r_associated | relid=0 | w=40
  143. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:lethal congenital contracture syndrome 2
    n1=en:chylomicron retention disease | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=40
  144. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:mannosidosis
    n1=en:chylomicron retention disease | n2=en:mannosidosis | rel=r_associated | relid=0 | w=40
  145. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:chylomicron retention disease | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=40
  146. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:chylomicron retention disease | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=40
  147. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:chylomicron retention disease | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=40
  148. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:morm syndrome
    n1=en:chylomicron retention disease | n2=en:morm syndrome | rel=r_associated | relid=0 | w=40
  149. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:chylomicron retention disease | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=40
  150. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:chylomicron retention disease | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=40
  151. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:nathalie syndrome
    n1=en:chylomicron retention disease | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=40
  152. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:neuroacanthocytosis
    n1=en:chylomicron retention disease | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=40
  153. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:niemann-pick disease
    n1=en:chylomicron retention disease | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=40
  154. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:chylomicron retention disease | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=40
  155. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:oculocutaneous albinism type 4
    n1=en:chylomicron retention disease | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=40
  156. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:peters-plus syndrome
    n1=en:chylomicron retention disease | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=40
  157. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:chylomicron retention disease | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=40
  158. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:prolonged electroretinal response suppression
    n1=en:chylomicron retention disease | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=40
  159. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:saito kuba tsuruta syndrome
    n1=en:chylomicron retention disease | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=40
  160. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:sar1b, 349, g-c, -1
    n1=en:chylomicron retention disease | n2=en:sar1b, 349, g-c, -1 | rel=r_associated | relid=0 | w=40
  161. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:chylomicron retention disease | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=40
  162. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:smith-mccort dysplasia
    n1=en:chylomicron retention disease | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=40
  163. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:chylomicron retention disease | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=40
  164. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:tay-sachs disease
    n1=en:chylomicron retention disease | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=40
  165. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:thyroid dyshormonogenesis 4
    n1=en:chylomicron retention disease | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=40
  166. en:chylomicron retention disease -- r_associated #0: 40 / 0.816 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:chylomicron retention disease | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=40
  167. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:absence of chylomicrons in lymph and plasma
    n1=en:chylomicron retention disease | n2=en:absence of chylomicrons in lymph and plasma | rel=r_associated | relid=0 | w=39
  168. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:alpha-fetoprotein deficiency
    n1=en:chylomicron retention disease | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=39
  169. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:alpha, alpha-trehalase deficiency
    n1=en:chylomicron retention disease | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=39
  170. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:chylomicron retention disease | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=39
  171. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:autosomal recessive ichthyosis
    n1=en:chylomicron retention disease | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=39
  172. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:beta-aminoisobutyricaciduria
    n1=en:chylomicron retention disease | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=39
  173. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:brody myopathy
    n1=en:chylomicron retention disease | n2=en:brody myopathy | rel=r_associated | relid=0 | w=39
  174. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:chondrodysplasia punctata syndrome
    n1=en:chylomicron retention disease | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=39
  175. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:classical phenylketonuria
    n1=en:chylomicron retention disease | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=39
  176. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:chylomicron retention disease | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=39
  177. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:cutis laxa, autosomal recessive
    n1=en:chylomicron retention disease | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=39
  178. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:cytochrome-c oxidase deficiency
    n1=en:chylomicron retention disease | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=39
  179. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:deficiency of glucosyltransferase 1
    n1=en:chylomicron retention disease | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=39
  180. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:chylomicron retention disease | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=39
  181. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:ehlers-danlos syndrome, type vi
    n1=en:chylomicron retention disease | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=39
  182. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:chylomicron retention disease | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=39
  183. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:fryns macrocephaly
    n1=en:chylomicron retention disease | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=39
  184. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:giacci familial neurogenic acroosteolysis
    n1=en:chylomicron retention disease | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=39
  185. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:hereditary fructose intolerance
    n1=en:chylomicron retention disease | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=39
  186. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=39
  187. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:hyperprolinemia type 1
    n1=en:chylomicron retention disease | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=39
  188. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:isolated hyperchlorhidrosis
    n1=en:chylomicron retention disease | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=39
  189. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:isolated hypoplasia of the right ventricle
    n1=en:chylomicron retention disease | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=39
  190. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:laurence-moon syndrome
    n1=en:chylomicron retention disease | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=39
  191. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:lecithin acyltransferase deficiency
    n1=en:chylomicron retention disease | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=39
  192. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:majeed syndrome
    n1=en:chylomicron retention disease | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=39
  193. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:malnutrition
    n1=en:chylomicron retention disease | n2=en:malnutrition | rel=r_associated | relid=0 | w=39
  194. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:multiple sulfatase deficiency disease
    n1=en:chylomicron retention disease | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=39
  195. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:myopathy with exercise intolerance, swedish type
    n1=en:chylomicron retention disease | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=39
  196. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:odontohypophosphatasia (disorder)
    n1=en:chylomicron retention disease | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  197. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:orotic aciduria
    n1=en:chylomicron retention disease | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=39
  198. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:papillon-lefevre syndrome
    n1=en:chylomicron retention disease | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=39
  199. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:pentosuria
    n1=en:chylomicron retention disease | n2=en:pentosuria | rel=r_associated | relid=0 | w=39
  200. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:phenylketonuria ii
    n1=en:chylomicron retention disease | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=39
  201. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:chylomicron retention disease | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=39
  202. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:presentey anomaly
    n1=en:chylomicron retention disease | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=39
  203. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:pseudocholinesterase deficiency
    n1=en:chylomicron retention disease | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=39
  204. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:sarcosinemia
    n1=en:chylomicron retention disease | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=39
  205. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:chylomicron retention disease | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=39
  206. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:chylomicron retention disease | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=39
  207. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:steatorrhea
    n1=en:chylomicron retention disease | n2=en:steatorrhea | rel=r_associated | relid=0 | w=39
  208. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:chylomicron retention disease | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=39
  209. en:chylomicron retention disease -- r_associated #0: 39 / 0.796 -> en:vomiting
    n1=en:chylomicron retention disease | n2=en:vomiting | rel=r_associated | relid=0 | w=39
  210. en:chylomicron retention disease -- r_associated #0: 38 / 0.776 -> en:hypomagnesemia 1, intestinal
    n1=en:chylomicron retention disease | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=38
  211. en:chylomicron retention disease -- r_associated #0: 38 / 0.776 -> rétention placentaire du postabortum
    n1=en:chylomicron retention disease | n2=rétention placentaire du postabortum | rel=r_associated | relid=0 | w=38
  212. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> Anderson (maladie d')
    n1=en:chylomicron retention disease | n2=Anderson (maladie d') | rel=r_associated | relid=0 | w=37
  213. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:albinotic fundus
    n1=en:chylomicron retention disease | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=37
  214. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:allanson pantzar mcleod syndrome
    n1=en:chylomicron retention disease | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=37
  215. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:chylomicron retention disease | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=37
  216. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:chylomicron retention disease | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=37
  217. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:chylomicron retention disease | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=37
  218. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:ataxia with vitamin e deficiency
    n1=en:chylomicron retention disease | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=37
  219. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:chylomicron retention disease | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=37
  220. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:biotinidase deficiency
    n1=en:chylomicron retention disease | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=37
  221. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:chylomicron retention disease | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=37
  222. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:citrin deficiency
    n1=en:chylomicron retention disease | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=37
  223. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:chylomicron retention disease | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=37
  224. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:combined malonic and methylmalonic aciduria
    n1=en:chylomicron retention disease | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=37
  225. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:corpus callosum agenesis neuronopathy
    n1=en:chylomicron retention disease | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=37
  226. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:crigler-najjar syndrome
    n1=en:chylomicron retention disease | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=37
  227. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:chylomicron retention disease | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=37
  228. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:deafness, sensorineural, and male infertility
    n1=en:chylomicron retention disease | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=37
  229. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:chylomicron retention disease | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=37
  230. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:enterokinase deficiency
    n1=en:chylomicron retention disease | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=37
  231. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37
  232. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:chylomicron retention disease | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=37
  233. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:isaacs syndrome
    n1=en:chylomicron retention disease | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=37
  234. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:kaufman-mckusick syndrome
    n1=en:chylomicron retention disease | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=37
  235. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:lethal congenital contracture syndrome type 3
    n1=en:chylomicron retention disease | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=37
  236. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:chylomicron retention disease | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=37
  237. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:chylomicron retention disease | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=37
  238. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:chylomicron retention disease | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=37
  239. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:malabsorption syndrome
    n1=en:chylomicron retention disease | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=37
  240. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:chylomicron retention disease | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=37
  241. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:muscle amp deaminase deficiency
    n1=en:chylomicron retention disease | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=37
  242. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:chylomicron retention disease | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=37
  243. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:nonaka myopathy
    n1=en:chylomicron retention disease | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=37
  244. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:otoonychoperoneal syndrome
    n1=en:chylomicron retention disease | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=37
  245. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:primary hyperoxaluria
    n1=en:chylomicron retention disease | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=37
  246. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:prolidase deficiency
    n1=en:chylomicron retention disease | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=37
  247. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:rapadilino syndrome
    n1=en:chylomicron retention disease | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=37
  248. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:sar1b, gly185val
    n1=en:chylomicron retention disease | n2=en:sar1b, gly185val | rel=r_associated | relid=0 | w=37
  249. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:chylomicron retention disease | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=37
  250. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:sonoda syndrome
    n1=en:chylomicron retention disease | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=37
  251. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:chylomicron retention disease | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=37
  252. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:chylomicron retention disease | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=37
  253. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:transcobalamin ii deficiency
    n1=en:chylomicron retention disease | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=37
  254. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:tyrosinemia type ii
    n1=en:chylomicron retention disease | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=37
  255. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:warsaw breakage syndrome
    n1=en:chylomicron retention disease | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=37
  256. en:chylomicron retention disease -- r_associated #0: 37 / 0.755 -> en:wolman disease
    n1=en:chylomicron retention disease | n2=en:wolman disease | rel=r_associated | relid=0 | w=37
  257. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:aminoacylase 1 deficiency
    n1=en:chylomicron retention disease | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=36
  258. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:ateliotic dwarfism without insulinopenia
    n1=en:chylomicron retention disease | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=36
  259. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:cohen syndrome
    n1=en:chylomicron retention disease | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=36
  260. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:congenital leptin deficiency
    n1=en:chylomicron retention disease | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=36
  261. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:deficiency of fat-soluble vitamins
    n1=en:chylomicron retention disease | n2=en:deficiency of fat-soluble vitamins | rel=r_associated | relid=0 | w=36
  262. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:desmosterolosis
    n1=en:chylomicron retention disease | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=36
  263. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:chylomicron retention disease | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=36
  264. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:ear, patella, short stature syndrome
    n1=en:chylomicron retention disease | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=36
  265. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:chylomicron retention disease | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=36
  266. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:chylomicron retention disease | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=36
  267. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:chylomicron retention disease | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=36
  268. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:chylomicron retention disease | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=36
  269. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:chylomicron retention disease | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=36
  270. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:hyperprolinemia type 2
    n1=en:chylomicron retention disease | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=36
  271. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:hypocholesterolemia
    n1=en:chylomicron retention disease | n2=en:hypocholesterolemia | rel=r_associated | relid=0 | w=36
  272. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:intestinal epithelial dysplasia
    n1=en:chylomicron retention disease | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=36
  273. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:lipoprotein glomerulopathy
    n1=en:chylomicron retention disease | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=36
  274. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:chylomicron retention disease | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=36
  275. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:naxos disease
    n1=en:chylomicron retention disease | n2=en:naxos disease | rel=r_associated | relid=0 | w=36
  276. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:neurologic deficits may occur secondarily to malabsorption
    n1=en:chylomicron retention disease | n2=en:neurologic deficits may occur secondarily to malabsorption | rel=r_associated | relid=0 | w=36
  277. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:chylomicron retention disease | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=36
  278. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:chylomicron retention disease | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=36
  279. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:sar1b, asp137asn
    n1=en:chylomicron retention disease | n2=en:sar1b, asp137asn | rel=r_associated | relid=0 | w=36
  280. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:chylomicron retention disease | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=36
  281. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:spondyloenchondrodysplasia
    n1=en:chylomicron retention disease | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=36
  282. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:waardenburg anophthalmia syndrome
    n1=en:chylomicron retention disease | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=36
  283. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:werdnig-hoffmann disease
    n1=en:chylomicron retention disease | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=36
  284. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> en:xanthinuria, type i
    n1=en:chylomicron retention disease | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=36
  285. en:chylomicron retention disease -- r_associated #0: 36 / 0.735 -> rétention membraneuse
    n1=en:chylomicron retention disease | n2=rétention membraneuse | rel=r_associated | relid=0 | w=36
  286. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:3-methylglutaconic aciduria type 1
    n1=en:chylomicron retention disease | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=35
  287. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:acrocallosal syndrome
    n1=en:chylomicron retention disease | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=35
  288. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:ataxia telangiectasia syndrome
    n1=en:chylomicron retention disease | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=35
  289. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:bothnia retinal dystrophy
    n1=en:chylomicron retention disease | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=35
  290. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:brown-vialetto-van laere syndrome
    n1=en:chylomicron retention disease | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=35
  291. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:cerebrotendinous xanthomatosis
    n1=en:chylomicron retention disease | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=35
  292. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:chylomicron retention disease | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=35
  293. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:decreased vibratory sense
    n1=en:chylomicron retention disease | n2=en:decreased vibratory sense | rel=r_associated | relid=0 | w=35
  294. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:familial acantholysis
    n1=en:chylomicron retention disease | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=35
  295. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:histidinemia
    n1=en:chylomicron retention disease | n2=en:histidinemia | rel=r_associated | relid=0 | w=35
  296. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:hypomyelination and congenital cataract
    n1=en:chylomicron retention disease | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=35
  297. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:knobloch syndrome
    n1=en:chylomicron retention disease | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=35
  298. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:leukotriene c4 synthase deficiency
    n1=en:chylomicron retention disease | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=35
  299. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:microcephalic primordial dwarfism toriello type
    n1=en:chylomicron retention disease | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=35
  300. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:sar1b, 2-bp del, 75tg
    n1=en:chylomicron retention disease | n2=en:sar1b, 2-bp del, 75tg | rel=r_associated | relid=0 | w=35
  301. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:chylomicron retention disease | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=35
  302. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:chylomicron retention disease | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=35
  303. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:valinemia
    n1=en:chylomicron retention disease | n2=en:valinemia | rel=r_associated | relid=0 | w=35
  304. en:chylomicron retention disease -- r_associated #0: 35 / 0.714 -> en:verloes bourguignon syndrome
    n1=en:chylomicron retention disease | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=35
  305. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:chylomicron retention disease | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=34
  306. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:argininemia
    n1=en:chylomicron retention disease | n2=en:argininemia | rel=r_associated | relid=0 | w=34
  307. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001)
    n1=en:chylomicron retention disease | n2=en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) | rel=r_associated | relid=0 | w=34
  308. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:chylomicron retention disease | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=34
  309. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:chylomicron retention disease | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=34
  310. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:chylomicron retention disease | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=34
  311. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:chylomicron retention disease | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=34
  312. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:chylomicron retention disease | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=34
  313. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:hereditary factor x deficiency disease
    n1=en:chylomicron retention disease | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=34
  314. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:hypospadias-mental retardation syndrome
    n1=en:chylomicron retention disease | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=34
  315. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:chylomicron retention disease | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=34
  316. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:chylomicron retention disease | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  317. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:chylomicron retention disease | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=34
  318. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:chylomicron retention disease | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=34
  319. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:small bowel enterocytes accumulate lipid droplets in membrane-bound compartments or in the cytoplasm
    n1=en:chylomicron retention disease | n2=en:small bowel enterocytes accumulate lipid droplets in membrane-bound compartments or in the cytoplasm | rel=r_associated | relid=0 | w=34
  320. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:sulfite oxidase deficiency
    n1=en:chylomicron retention disease | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=34
  321. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:trichohepatoenteric syndrome
    n1=en:chylomicron retention disease | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=34
  322. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:tyrosinemia, type iii
    n1=en:chylomicron retention disease | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=34
  323. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> en:uv-sensitive syndrome
    n1=en:chylomicron retention disease | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=34
  324. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> rétention des chylomicrons (maladie de la)
    n1=en:chylomicron retention disease | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=34
  325. en:chylomicron retention disease -- r_associated #0: 34 / 0.694 -> rétention hydrochlorurée sodique
    n1=en:chylomicron retention disease | n2=rétention hydrochlorurée sodique | rel=r_associated | relid=0 | w=34
  326. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:autosomal recessive primary microcephaly
    n1=en:chylomicron retention disease | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=33
  327. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:bowen-conradi syndrome
    n1=en:chylomicron retention disease | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=33
  328. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:i-cell disease
    n1=en:chylomicron retention disease | n2=en:i-cell disease | rel=r_associated | relid=0 | w=33
  329. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:infantile onset
    n1=en:chylomicron retention disease | n2=en:infantile onset | rel=r_associated | relid=0 | w=33
  330. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:laron syndrome
    n1=en:chylomicron retention disease | n2=en:laron syndrome | rel=r_associated | relid=0 | w=33
  331. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:propionic acidemia
    n1=en:chylomicron retention disease | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=33
  332. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:spondylo-ocular syndrome
    n1=en:chylomicron retention disease | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=33
  333. en:chylomicron retention disease -- r_associated #0: 33 / 0.673 -> en:tetra-amelia autosomal recessive
    n1=en:chylomicron retention disease | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=33
  334. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:autosomal recessive asexual dwarfism
    n1=en:chylomicron retention disease | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=32
  335. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:chylomicron retention disease | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=32
  336. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:crisponi syndrome
    n1=en:chylomicron retention disease | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=32
  337. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:donnai-barrow syndrome
    n1=en:chylomicron retention disease | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=32
  338. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:chylomicron retention disease | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=32
  339. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:chylomicron retention disease | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=32
  340. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:neonatal progeroid syndrome
    n1=en:chylomicron retention disease | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=32
  341. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:netherton syndrome
    n1=en:chylomicron retention disease | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=32
  342. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:north american indian childhood cirrhosis
    n1=en:chylomicron retention disease | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=32
  343. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:persistent mullerian duct syndrome
    n1=en:chylomicron retention disease | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=32
  344. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:richards-rundle syndrome
    n1=en:chylomicron retention disease | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=32
  345. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:severe early childhood onset retinal dystrophy
    n1=en:chylomicron retention disease | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=32
  346. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:sly syndrome
    n1=en:chylomicron retention disease | n2=en:sly syndrome | rel=r_associated | relid=0 | w=32
  347. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> en:spinocerebellar ataxia with epilepsy
    n1=en:chylomicron retention disease | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=32
  348. en:chylomicron retention disease -- r_associated #0: 32 / 0.653 -> rétentionniste
    n1=en:chylomicron retention disease | n2=rétentionniste | rel=r_associated | relid=0 | w=32
  349. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:autosomal recessive sideroblastic anemia
    n1=en:chylomicron retention disease | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=31
  350. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:charcot-marie-tooth disease type 4
    n1=en:chylomicron retention disease | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=31
  351. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:hepatolenticular degeneration
    n1=en:chylomicron retention disease | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=31
  352. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:microcephaly cervical spine fusion anomalies
    n1=en:chylomicron retention disease | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=31
  353. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:sar1b, ser179arg
    n1=en:chylomicron retention disease | n2=en:sar1b, ser179arg | rel=r_associated | relid=0 | w=31
  354. en:chylomicron retention disease -- r_associated #0: 31 / 0.633 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:chylomicron retention disease | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=31
  355. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> en:allgrove syndrome
    n1=en:chylomicron retention disease | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=30
  356. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> en:maple syrup urine disease
    n1=en:chylomicron retention disease | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=30
  357. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> en:xeroderma pigmentosum
    n1=en:chylomicron retention disease | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=30
  358. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> médecine
    n1=en:chylomicron retention disease | n2=médecine | rel=r_associated | relid=0 | w=30
  359. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> rétention sudorale
    n1=en:chylomicron retention disease | n2=rétention sudorale | rel=r_associated | relid=0 | w=30
  360. en:chylomicron retention disease -- r_associated #0: 30 / 0.612 -> vomissement
    n1=en:chylomicron retention disease | n2=vomissement | rel=r_associated | relid=0 | w=30
  361. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:3-methylglutaconic aciduria type 5
    n1=en:chylomicron retention disease | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=29
  362. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:fucosidosis
    n1=en:chylomicron retention disease | n2=en:fucosidosis | rel=r_associated | relid=0 | w=29
  363. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:gamma-glutamyltransferase deficiency
    n1=en:chylomicron retention disease | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=29
  364. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:glycogen storage disease type x
    n1=en:chylomicron retention disease | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=29
  365. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:maroteaux-lamy syndrome
    n1=en:chylomicron retention disease | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=29
  366. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:peeling skin syndrome, acral type
    n1=en:chylomicron retention disease | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=29
  367. en:chylomicron retention disease -- r_associated #0: 29 / 0.592 -> en:pyle metaphyseal dysplasia
    n1=en:chylomicron retention disease | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=29
  368. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:al awadi syndrome
    n1=en:chylomicron retention disease | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=28
  369. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:chylomicron retention disease | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=28
  370. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:cerebellar ataxia, cayman type
    n1=en:chylomicron retention disease | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=28
  371. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:deficiency of fructokinase
    n1=en:chylomicron retention disease | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=28
  372. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:chylomicron retention disease | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=28
  373. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:hnsha due to aldolase a deficiency
    n1=en:chylomicron retention disease | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=28
  374. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:hypokalemia, familial
    n1=en:chylomicron retention disease | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=28
  375. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:jankovic rivera syndrome
    n1=en:chylomicron retention disease | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=28
  376. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:sweat retention
    n1=en:chylomicron retention disease | n2=en:sweat retention | rel=r_associated | relid=0 | w=28
  377. en:chylomicron retention disease -- r_associated #0: 28 / 0.571 -> en:urocanase deficiency
    n1=en:chylomicron retention disease | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=28
  378. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:behr syndrome
    n1=en:chylomicron retention disease | n2=en:behr syndrome | rel=r_associated | relid=0 | w=27
  379. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:congenital disorder of glycosylation type ig
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=27
  380. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:chylomicron retention disease | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=27
  381. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:hyperlipoproteinemia type i
    n1=en:chylomicron retention disease | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=27
  382. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:intestinal malabsorption of fat
    n1=en:chylomicron retention disease | n2=en:intestinal malabsorption of fat | rel=r_associated | relid=0 | w=27
  383. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:chylomicron retention disease | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=27
  384. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> en:thomas syndrome
    n1=en:chylomicron retention disease | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=27
  385. en:chylomicron retention disease -- r_associated #0: 27 / 0.551 -> hyperchylomicronémie
    n1=en:chylomicron retention disease | n2=hyperchylomicronémie | rel=r_associated | relid=0 | w=27
  386. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:5-oxoprolinase deficiency
    n1=en:chylomicron retention disease | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=26
  387. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:familial hypoaldosteronism
    n1=en:chylomicron retention disease | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=26
  388. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:glutamate formiminotransferase deficiency
    n1=en:chylomicron retention disease | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=26
  389. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:growth retardation
    n1=en:chylomicron retention disease | n2=en:growth retardation | rel=r_associated | relid=0 | w=26
  390. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:hypobetalipoproteinemias
    n1=en:chylomicron retention disease | n2=en:hypobetalipoproteinemias | rel=r_associated | relid=0 | w=26
  391. en:chylomicron retention disease -- r_associated #0: 26 / 0.531 -> en:missed abortion
    n1=en:chylomicron retention disease | n2=en:missed abortion | rel=r_associated | relid=0 | w=26
  392. en:chylomicron retention disease -- r_associated #0: 24 / 0.49 -> maladie
    n1=en:chylomicron retention disease | n2=maladie | rel=r_associated | relid=0 | w=24
  393. en:chylomicron retention disease -- r_associated #0: 23 / 0.469 -> en:membranous retention
    n1=en:chylomicron retention disease | n2=en:membranous retention | rel=r_associated | relid=0 | w=23
  394. en:chylomicron retention disease -- r_associated #0: 22 / 0.449 -> chylomicrons
    n1=en:chylomicron retention disease | n2=chylomicrons | rel=r_associated | relid=0 | w=22
  395. en:chylomicron retention disease -- r_associated #0: 22 / 0.449 -> en:retained placenta
    n1=en:chylomicron retention disease | n2=en:retained placenta | rel=r_associated | relid=0 | w=22
  396. en:chylomicron retention disease -- r_associated #0: 22 / 0.449 -> rétention
    n1=en:chylomicron retention disease | n2=rétention | rel=r_associated | relid=0 | w=22
  397. en:chylomicron retention disease -- r_associated #0: 21 / 0.429 -> en:placental retention
    n1=en:chylomicron retention disease | n2=en:placental retention | rel=r_associated | relid=0 | w=21
  398. en:chylomicron retention disease -- r_associated #0: 21 / 0.429 -> en:retentionist
    n1=en:chylomicron retention disease | n2=en:retentionist | rel=r_associated | relid=0 | w=21
  399. en:chylomicron retention disease -- r_associated #0: 21 / 0.429 -> syndrome de Walker-Warburg
    n1=en:chylomicron retention disease | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=21
  400. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> a-bêta-lipoprotéinémie
    n1=en:chylomicron retention disease | n2=a-bêta-lipoprotéinémie | rel=r_associated | relid=0 | w=20
  401. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> abêtalipoprotéinémie
    n1=en:chylomicron retention disease | n2=abêtalipoprotéinémie | rel=r_associated | relid=0 | w=20
  402. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> abêtalipoprotéinémie normotriglycéridémique de type Steinberg
    n1=en:chylomicron retention disease | n2=abêtalipoprotéinémie normotriglycéridémique de type Steinberg | rel=r_associated | relid=0 | w=20
  403. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> absence de croissance
    n1=en:chylomicron retention disease | n2=absence de croissance | rel=r_associated | relid=0 | w=20
  404. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> acrodermatite entéropathique
    n1=en:chylomicron retention disease | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  405. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> adénite sinusale cytophagique
    n1=en:chylomicron retention disease | n2=adénite sinusale cytophagique | rel=r_associated | relid=0 | w=20
  406. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> asthénie sénile
    n1=en:chylomicron retention disease | n2=asthénie sénile | rel=r_associated | relid=0 | w=20
  407. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> débilité sénile
    n1=en:chylomicron retention disease | n2=débilité sénile | rel=r_associated | relid=0 | w=20
  408. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en céto-acide décarboxylase
    n1=en:chylomicron retention disease | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  409. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en cytochrome oxydase
    n1=en:chylomicron retention disease | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  410. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en cytochrome-c oxydase
    n1=en:chylomicron retention disease | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  411. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en neuraminidase
    n1=en:chylomicron retention disease | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20
  412. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en prolidase
    n1=en:chylomicron retention disease | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  413. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en pyruvate carboxylase
    n1=en:chylomicron retention disease | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  414. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:chylomicron retention disease | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  415. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> déficit en sulfite-oxydase
    n1=en:chylomicron retention disease | n2=déficit en sulfite-oxydase | rel=r_associated | relid=0 | w=20
  416. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence (sémiologie)
    n1=en:chylomicron retention disease | n2=démence (sémiologie) | rel=r_associated | relid=0 | w=20
  417. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence dégénérative primaire
    n1=en:chylomicron retention disease | n2=démence dégénérative primaire | rel=r_associated | relid=0 | w=20
  418. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence forme dépressive ou délirante
    n1=en:chylomicron retention disease | n2=démence forme dépressive ou délirante | rel=r_associated | relid=0 | w=20
  419. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence présénile
    n1=en:chylomicron retention disease | n2=démence présénile | rel=r_associated | relid=0 | w=20
  420. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence sénile
    n1=en:chylomicron retention disease | n2=démence sénile | rel=r_associated | relid=0 | w=20
  421. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> démence sénile avec delirium ou état confusionnel aigu
    n1=en:chylomicron retention disease | n2=démence sénile avec delirium ou état confusionnel aigu | rel=r_associated | relid=0 | w=20
  422. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> dysplasie craniodiaphysaire
    n1=en:chylomicron retention disease | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20
  423. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:abetalipoproteinemia
    n1=en:chylomicron retention disease | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=20
  424. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:acrorenal mandibular syndrome
    n1=en:chylomicron retention disease | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  425. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:chylomicron retention disease | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  426. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:chylomicron retention disease | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  427. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:age-related physical debility
    n1=en:chylomicron retention disease | n2=en:age-related physical debility | rel=r_associated | relid=0 | w=20
  428. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:anauxetic dysplasia
    n1=en:chylomicron retention disease | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20
  429. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:autosomal recessive spastic paraplegia type 39
    n1=en:chylomicron retention disease | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20
  430. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:bamforth syndrome
    n1=en:chylomicron retention disease | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  431. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Bassen-Kornzweig disease
    n1=en:chylomicron retention disease | n2=en:Bassen-Kornzweig disease | rel=r_associated | relid=0 | w=20
  432. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Bassen-Kornzweig's disease
    n1=en:chylomicron retention disease | n2=en:Bassen-Kornzweig's disease | rel=r_associated | relid=0 | w=20
  433. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:bestrophinopathy, autosomal recessive
    n1=en:chylomicron retention disease | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20
  434. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:braddock syndrome
    n1=en:chylomicron retention disease | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  435. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:brain calcification rajab type
    n1=en:chylomicron retention disease | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  436. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:branched-chain ketoaciduria
    n1=en:chylomicron retention disease | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  437. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:chylomicron retention disease | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  438. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:classical maple syrup urine disease
    n1=en:chylomicron retention disease | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  439. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital analbuminemia
    n1=en:chylomicron retention disease | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  440. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:chylomicron retention disease | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  441. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital disorder of glycosylation type 1h
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20
  442. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital disorder of glycosylation type 2e
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20
  443. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital disorder of glycosylation type id
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20
  444. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital disorder of glycosylation type ie
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20
  445. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:congenital disorder of glycosylation, type if
    n1=en:chylomicron retention disease | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20
  446. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:cooper jabs syndrome
    n1=en:chylomicron retention disease | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  447. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:craniofacial ulnar renal syndrome
    n1=en:chylomicron retention disease | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20
  448. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Crigler Najjar's disease
    n1=en:chylomicron retention disease | n2=en:Crigler Najjar's disease | rel=r_associated | relid=0 | w=20
  449. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:chylomicron retention disease | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  450. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:deafness and myopia syndrome
    n1=en:chylomicron retention disease | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  451. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:chylomicron retention disease | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  452. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:diaphanospondylodysostosis
    n1=en:chylomicron retention disease | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20
  453. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Dubin-Johnson's syndrome
    n1=en:chylomicron retention disease | n2=en:Dubin-Johnson's syndrome | rel=r_associated | relid=0 | w=20
  454. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:chylomicron retention disease | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  455. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type
    n1=en:chylomicron retention disease | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
  456. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:familial median cleft of upper and lower lip
    n1=en:chylomicron retention disease | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  457. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:fountain syndrome
    n1=en:chylomicron retention disease | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  458. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:generalized peeling skin syndrome
    n1=en:chylomicron retention disease | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  459. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    n1=en:chylomicron retention disease | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20
  460. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:hall riggs syndrome
    n1=en:chylomicron retention disease | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  461. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:heart defects limb shortening
    n1=en:chylomicron retention disease | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  462. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:histidinaemia
    n1=en:chylomicron retention disease | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20
  463. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:hyperchylomicronaemia
    n1=en:chylomicron retention disease | n2=en:hyperchylomicronaemia | rel=r_associated | relid=0 | w=20
  464. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:hyperlipoproteinemia type I
    n1=en:chylomicron retention disease | n2=en:hyperlipoproteinemia type I | rel=r_associated | relid=0 | w=20
  465. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:hypomandibular faciocranial dysostosis
    n1=en:chylomicron retention disease | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  466. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:hypophosphatasia infantile
    n1=en:chylomicron retention disease | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  467. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:I-cell disease
    n1=en:chylomicron retention disease | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20
  468. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:insulin growth factor i deficiency
    n1=en:chylomicron retention disease | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  469. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:kallman syndrome with heart disease
    n1=en:chylomicron retention disease | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  470. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:late-onset junctional epidermolysis bullosa
    n1=en:chylomicron retention disease | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  471. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Laurence-Moon's syndrome
    n1=en:chylomicron retention disease | n2=en:Laurence-Moon's syndrome | rel=r_associated | relid=0 | w=20
  472. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Leroy's i-cell disease
    n1=en:chylomicron retention disease | n2=en:Leroy's i-cell disease | rel=r_associated | relid=0 | w=20
  473. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:lethal larsen-like syndrome
    n1=en:chylomicron retention disease | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20
  474. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:leucinosis
    n1=en:chylomicron retention disease | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  475. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:chylomicron retention disease | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  476. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:manouvrier syndrome
    n1=en:chylomicron retention disease | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  477. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:maple-tree syrup disease
    n1=en:chylomicron retention disease | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  478. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
    n1=en:chylomicron retention disease | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20
  479. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:chylomicron retention disease | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  480. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:chylomicron retention disease | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  481. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:moyamoya disease with early onset achalasia
    n1=en:chylomicron retention disease | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  482. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:mucopolysaccharidosis i
    n1=en:chylomicron retention disease | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20
  483. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:najjar syndrome
    n1=en:chylomicron retention disease | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  484. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Niemann-Pick disease
    n1=en:chylomicron retention disease | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20
  485. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:oculocutaneous albinism type 6
    n1=en:chylomicron retention disease | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20
  486. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:chylomicron retention disease | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  487. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:pelviscapular dysplasia
    n1=en:chylomicron retention disease | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  488. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:pili torti onychodysplasia syndrome
    n1=en:chylomicron retention disease | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
  489. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:presenile dementia
    n1=en:chylomicron retention disease | n2=en:presenile dementia | rel=r_associated | relid=0 | w=20
  490. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:primary immunodeficiency syndrome due to p14 deficiency
    n1=en:chylomicron retention disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20
  491. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:renal dysplasia - limb defects syndrome
    n1=en:chylomicron retention disease | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  492. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:robinow-like syndrome
    n1=en:chylomicron retention disease | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  493. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:senile asthenia
    n1=en:chylomicron retention disease | n2=en:senile asthenia | rel=r_associated | relid=0 | w=20
  494. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:senile dementia
    n1=en:chylomicron retention disease | n2=en:senile dementia | rel=r_associated | relid=0 | w=20
  495. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:senility
    n1=en:chylomicron retention disease | n2=en:senility | rel=r_associated | relid=0 | w=20
  496. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:split-hand/foot malformation 3
    n1=en:chylomicron retention disease | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  497. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:chylomicron retention disease | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  498. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
    n1=en:chylomicron retention disease | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20
  499. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Tay-Sachs disease
    n1=en:chylomicron retention disease | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  500. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:thiamin-responsive maple syrup urine disease
    n1=en:chylomicron retention disease | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  501. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:unspecified senile psychotic condition
    n1=en:chylomicron retention disease | n2=en:unspecified senile psychotic condition | rel=r_associated | relid=0 | w=20
  502. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:vomitus
    n1=en:chylomicron retention disease | n2=en:vomitus | rel=r_associated | relid=0 | w=20
  503. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Wolman's disease
    n1=en:chylomicron retention disease | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  504. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:chylomicron retention disease | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  505. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:Zellweger syndrome
    n1=en:chylomicron retention disease | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  506. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> en:zellweger-like syndrome without peroxisomal anomaly
    n1=en:chylomicron retention disease | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20
  507. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> fucosidose
    n1=en:chylomicron retention disease | n2=fucosidose | rel=r_associated | relid=0 | w=20
  508. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hérédité autosomale récessive
    n1=en:chylomicron retention disease | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  509. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> histidinémie
    n1=en:chylomicron retention disease | n2=histidinémie | rel=r_associated | relid=0 | w=20
  510. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> histiocytose sinusale hémophagocytaire
    n1=en:chylomicron retention disease | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20
  511. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hyperoxalurie primaire
    n1=en:chylomicron retention disease | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  512. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hyperoxalurie primitive
    n1=en:chylomicron retention disease | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  513. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hyperplasie congénitale des surrénales
    n1=en:chylomicron retention disease | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  514. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hypo-bêta-lipoprotéinémie
    n1=en:chylomicron retention disease | n2=hypo-bêta-lipoprotéinémie | rel=r_associated | relid=0 | w=20
  515. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hypo-bêtalipoprotéinémie
    n1=en:chylomicron retention disease | n2=hypo-bêtalipoprotéinémie | rel=r_associated | relid=0 | w=20
  516. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hypobêtalipoprotéinémie
    n1=en:chylomicron retention disease | n2=hypobêtalipoprotéinémie | rel=r_associated | relid=0 | w=20
  517. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hypophosphatasie foetale
    n1=en:chylomicron retention disease | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  518. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> hypophosphatasie infantile
    n1=en:chylomicron retention disease | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  519. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> intolérance au fructose
    n1=en:chylomicron retention disease | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  520. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> leucinose
    n1=en:chylomicron retention disease | n2=leucinose | rel=r_associated | relid=0 | w=20
  521. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de Crigler-Najjar
    n1=en:chylomicron retention disease | n2=maladie de Crigler-Najjar | rel=r_associated | relid=0 | w=20
  522. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de Niemann-Pick
    n1=en:chylomicron retention disease | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20
  523. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de Tay-Sachs
    n1=en:chylomicron retention disease | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  524. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de tay-sachs
    n1=en:chylomicron retention disease | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  525. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de Tay-sachs
    n1=en:chylomicron retention disease | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  526. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de wolman
    n1=en:chylomicron retention disease | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  527. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> Maladie de Wolman
    n1=en:chylomicron retention disease | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20
  528. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie de Wolman
    n1=en:chylomicron retention disease | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  529. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:chylomicron retention disease | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  530. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie des urines avec odeur de sirop erable
    n1=en:chylomicron retention disease | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  531. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> maladie du sirop d'érable
    n1=en:chylomicron retention disease | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  532. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> mucolipidose II
    n1=en:chylomicron retention disease | n2=mucolipidose II | rel=r_associated | relid=0 | w=20
  533. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> mucolipidose type ii
    n1=en:chylomicron retention disease | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20
  534. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> mucolipidose type II
    n1=en:chylomicron retention disease | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20
  535. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> mucopolysaccharidose de type I
    n1=en:chylomicron retention disease | n2=mucopolysaccharidose de type I | rel=r_associated | relid=0 | w=20
  536. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> neuro-acanthocytose
    n1=en:chylomicron retention disease | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  537. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> oxalose
    n1=en:chylomicron retention disease | n2=oxalose | rel=r_associated | relid=0 | w=20
  538. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> oxalose primitive
    n1=en:chylomicron retention disease | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  539. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> oxaloses
    n1=en:chylomicron retention disease | n2=oxaloses | rel=r_associated | relid=0 | w=20
  540. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> psychose présénile
    n1=en:chylomicron retention disease | n2=psychose présénile | rel=r_associated | relid=0 | w=20
  541. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> psychose sénile
    n1=en:chylomicron retention disease | n2=psychose sénile | rel=r_associated | relid=0 | w=20
  542. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> retard de croissance
    n1=en:chylomicron retention disease | n2=retard de croissance | rel=r_associated | relid=0 | w=20
  543. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> retard de croissance staturo-pondérale
    n1=en:chylomicron retention disease | n2=retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  544. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> Retard de croissance staturo-pondérale
    n1=en:chylomicron retention disease | n2=Retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  545. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> sénescence sans mention de psychose
    n1=en:chylomicron retention disease | n2=sénescence sans mention de psychose | rel=r_associated | relid=0 | w=20
  546. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> sénilité
    n1=en:chylomicron retention disease | n2=sénilité | rel=r_associated | relid=0 | w=20
  547. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> sirop d'érable (urine à odeur de)
    n1=en:chylomicron retention disease | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  548. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de dubin-johnson
    n1=en:chylomicron retention disease | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  549. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de Dubin-Johnson
    n1=en:chylomicron retention disease | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  550. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de glissement
    n1=en:chylomicron retention disease | n2=syndrome de glissement | rel=r_associated | relid=0 | w=20
  551. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de Laurence-Moon
    n1=en:chylomicron retention disease | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  552. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de malabsorption
    n1=en:chylomicron retention disease | n2=syndrome de malabsorption | rel=r_associated | relid=0 | w=20
  553. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome de synostose spondylo-carpo-tarsale
    n1=en:chylomicron retention disease | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20
  554. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> syndrome du retard de développement
    n1=en:chylomicron retention disease | n2=syndrome du retard de développement | rel=r_associated | relid=0 | w=20
  555. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> trouble psychotique sénile non précisé
    n1=en:chylomicron retention disease | n2=trouble psychotique sénile non précisé | rel=r_associated | relid=0 | w=20
  556. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> v+
    n1=en:chylomicron retention disease | n2=v+ | rel=r_associated | relid=0 | w=20
  557. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> V+
    n1=en:chylomicron retention disease | n2=V+ | rel=r_associated | relid=0 | w=20
  558. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:chylomicron retention disease | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  559. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> vieillesse sans mention de psychose
    n1=en:chylomicron retention disease | n2=vieillesse sans mention de psychose | rel=r_associated | relid=0 | w=20
  560. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> vomissements
    n1=en:chylomicron retention disease | n2=vomissements | rel=r_associated | relid=0 | w=20
  561. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> Walker-Warburg (syndrome de)
    n1=en:chylomicron retention disease | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  562. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> Wolman (maladie de)
    n1=en:chylomicron retention disease | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  563. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xanthique (lithiase)
    n1=en:chylomicron retention disease | n2=xanthique (lithiase) | rel=r_associated | relid=0 | w=20
  564. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xanthomatose cérébro-tendineuse
    n1=en:chylomicron retention disease | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  565. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xanthomatose cérébrotendineuse
    n1=en:chylomicron retention disease | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  566. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:chylomicron retention disease | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  567. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xeroderma pigmentosum
    n1=en:chylomicron retention disease | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  568. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> Xeroderma pigmentosum
    n1=en:chylomicron retention disease | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  569. en:chylomicron retention disease -- r_associated #0: 20 / 0.408 -> xérodermite pigmentaire
    n1=en:chylomicron retention disease | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
  570. en:chylomicron retention disease -- r_associated #0: 15 / 0.306 -> maladies
    n1=en:chylomicron retention disease | n2=maladies | rel=r_associated | relid=0 | w=15
  571. en:chylomicron retention disease -- r_associated #0: 11 / 0.224 -> processus pathologique
    n1=en:chylomicron retention disease | n2=processus pathologique | rel=r_associated | relid=0 | w=11
  572. en:chylomicron retention disease -- r_associated #0: 10 / 0.204 -> placentaire
    n1=en:chylomicron retention disease | n2=placentaire | rel=r_associated | relid=0 | w=10
  573. en:chylomicron retention disease -- r_associated #0: 1 / 0.02 -> maladie
    (médecine)
    n1=en:chylomicron retention disease | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=1
≈ 717 relations entrantes

  1. en:vomiting --- r_associated #0: 450 --> en:chylomicron retention disease
    n1=en:vomiting | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=450
  2. vomissement --- r_associated #0: 448 --> en:chylomicron retention disease
    n1=vomissement | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=448
  3. démence dégénérative primaire --- r_associated #0: 420 --> en:chylomicron retention disease
    n1=démence dégénérative primaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=420
  4. psychose présénile --- r_associated #0: 420 --> en:chylomicron retention disease
    n1=psychose présénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=420
  5. trouble psychotique sénile non précisé --- r_associated #0: 420 --> en:chylomicron retention disease
    n1=trouble psychotique sénile non précisé | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=420
  6. psychose sénile --- r_associated #0: 418 --> en:chylomicron retention disease
    n1=psychose sénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=418
  7. asthénie sénile --- r_associated #0: 415 --> en:chylomicron retention disease
    n1=asthénie sénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=415
  8. démence forme dépressive ou délirante --- r_associated #0: 415 --> en:chylomicron retention disease
    n1=démence forme dépressive ou délirante | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=415
  9. démence sénile avec delirium ou état confusionnel aigu --- r_associated #0: 415 --> en:chylomicron retention disease
    n1=démence sénile avec delirium ou état confusionnel aigu | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=415
  10. sénescence sans mention de psychose --- r_associated #0: 415 --> en:chylomicron retention disease
    n1=sénescence sans mention de psychose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=415
  11. débilité sénile --- r_associated #0: 410 --> en:chylomicron retention disease
    n1=débilité sénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=410
  12. en:unspecified senile psychotic condition --- r_associated #0: 410 --> en:chylomicron retention disease
    n1=en:unspecified senile psychotic condition | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=410
  13. vieillesse sans mention de psychose --- r_associated #0: 408 --> en:chylomicron retention disease
    n1=vieillesse sans mention de psychose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=408
  14. en:senile asthenia --- r_associated #0: 405 --> en:chylomicron retention disease
    n1=en:senile asthenia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=405
  15. en:senility --- r_associated #0: 405 --> en:chylomicron retention disease
    n1=en:senility | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=405
  16. démence présénile --- r_associated #0: 396 --> en:chylomicron retention disease
    n1=démence présénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=396
  17. en:age-related physical debility --- r_associated #0: 390 --> en:chylomicron retention disease
    n1=en:age-related physical debility | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=390
  18. syndrome de glissement --- r_associated #0: 385 --> en:chylomicron retention disease
    n1=syndrome de glissement | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=385
  19. démence sénile --- r_associated #0: 375 --> en:chylomicron retention disease
    n1=démence sénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=375
  20. en:presenile dementia --- r_associated #0: 375 --> en:chylomicron retention disease
    n1=en:presenile dementia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=375
  21. sénilité --- r_associated #0: 368 --> en:chylomicron retention disease
    n1=sénilité | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=368
  22. hypophosphatasie infantile --- r_associated #0: 213 --> en:chylomicron retention disease
    n1=hypophosphatasie infantile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=213
  23. en:infantile hypophosphatasia --- r_associated #0: 212 --> en:chylomicron retention disease
    n1=en:infantile hypophosphatasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=212
  24. hypophosphatasie foetale --- r_associated #0: 211 --> en:chylomicron retention disease
    n1=hypophosphatasie foetale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=211
  25. hypo-bêta-lipoprotéinémie --- r_associated #0: 206 --> en:chylomicron retention disease
    n1=hypo-bêta-lipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=206
  26. hypo-bêtalipoprotéinémie --- r_associated #0: 205 --> en:chylomicron retention disease
    n1=hypo-bêtalipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=205
  27. hypobêtalipoprotéinémie --- r_associated #0: 205 --> en:chylomicron retention disease
    n1=hypobêtalipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=205
  28. en:hypobetalipoproteinemias --- r_associated #0: 203 --> en:chylomicron retention disease
    n1=en:hypobetalipoproteinemias | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=203
  29. a-bêta-lipoprotéinémie --- r_associated #0: 180 --> en:chylomicron retention disease
    n1=a-bêta-lipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=180
  30. abêtalipoprotéinémie --- r_associated #0: 180 --> en:chylomicron retention disease
    n1=abêtalipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=180
  31. en:abetalipoproteinemia --- r_associated #0: 180 --> en:chylomicron retention disease
    n1=en:abetalipoproteinemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=180
  32. en:walker-warburg syndrome --- r_associated #0: 180 --> en:chylomicron retention disease
    n1=en:walker-warburg syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=180
  33. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:chylomicron retention disease
    n1=syndrome de Walker-Warburg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=178
  34. en:pyruvate carboxylase deficiency --- r_associated #0: 175 --> en:chylomicron retention disease
    n1=en:pyruvate carboxylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=175
  35. déficit en pyruvate carboxylase --- r_associated #0: 174 --> en:chylomicron retention disease
    n1=déficit en pyruvate carboxylase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=174
  36. en:xeroderma pigmentosum --- r_associated #0: 174 --> en:chylomicron retention disease
    n1=en:xeroderma pigmentosum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=174
  37. xeroderma pigmentosum --- r_associated #0: 170 --> en:chylomicron retention disease
    n1=xeroderma pigmentosum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=170
  38. en:zellweger syndrome --- r_associated #0: 169 --> en:chylomicron retention disease
    n1=en:zellweger syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=169
  39. en:Zellweger syndrome --- r_associated #0: 165 --> en:chylomicron retention disease
    n1=en:Zellweger syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=165
  40. retard de croissance staturo-pondérale --- r_associated #0: 146 --> en:chylomicron retention disease
    n1=retard de croissance staturo-pondérale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=146
  41. en:pediatric failure to thrive --- r_associated #0: 145 --> en:chylomicron retention disease
    n1=en:pediatric failure to thrive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=145
  42. Retard de croissance staturo-pondérale --- r_associated #0: 140 --> en:chylomicron retention disease
    n1=Retard de croissance staturo-pondérale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=140
  43. absence de croissance --- r_associated #0: 140 --> en:chylomicron retention disease
    n1=absence de croissance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=140
  44. syndrome du retard de développement --- r_associated #0: 140 --> en:chylomicron retention disease
    n1=syndrome du retard de développement | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=140
  45. vomissements --- r_associated #0: 114 --> en:chylomicron retention disease
    n1=vomissements | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=114
  46. en:primary hyperoxaluria --- r_associated #0: 111 --> en:chylomicron retention disease
    n1=en:primary hyperoxaluria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=111
  47. hyperoxalurie primaire --- r_associated #0: 111 --> en:chylomicron retention disease
    n1=hyperoxalurie primaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=111
  48. oxalose primitive --- r_associated #0: 111 --> en:chylomicron retention disease
    n1=oxalose primitive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=111
  49. oxaloses --- r_associated #0: 111 --> en:chylomicron retention disease
    n1=oxaloses | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=111
  50. hyperoxalurie primitive --- r_associated #0: 110 --> en:chylomicron retention disease
    n1=hyperoxalurie primitive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=110
  51. déficit en cytochrome oxydase --- r_associated #0: 109 --> en:chylomicron retention disease
    n1=déficit en cytochrome oxydase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=109
  52. en:cytochrome-c oxidase deficiency --- r_associated #0: 109 --> en:chylomicron retention disease
    n1=en:cytochrome-c oxidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=109
  53. oxalose --- r_associated #0: 105 --> en:chylomicron retention disease
    n1=oxalose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=105
  54. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:chylomicron retention disease
    n1=déficit en cytochrome-c oxydase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=95
  55. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:chylomicron retention disease
    n1=hyperplasie congénitale des surrénales | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=95
  56. en:congenital adrenal hyperplasia --- r_associated #0: 93 --> en:chylomicron retention disease
    n1=en:congenital adrenal hyperplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=93
  57. retard de croissance --- r_associated #0: 74 --> en:chylomicron retention disease
    n1=retard de croissance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=74
  58. en:i-cell disease --- r_associated #0: 61 --> en:chylomicron retention disease
    n1=en:i-cell disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=61
  59. en:I-cell disease --- r_associated #0: 59 --> en:chylomicron retention disease
    n1=en:I-cell disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=59
  60. Xeroderma pigmentosum --- r_associated #0: 55 --> en:chylomicron retention disease
    n1=Xeroderma pigmentosum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=55
  61. en:tay-sachs disease --- r_associated #0: 53 --> en:chylomicron retention disease
    n1=en:tay-sachs disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=53
  62. en:wolman disease --- r_associated #0: 51 --> en:chylomicron retention disease
    n1=en:wolman disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=51
  63. maladie de Wolman --- r_associated #0: 51 --> en:chylomicron retention disease
    n1=maladie de Wolman | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=51
  64. xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:chylomicron retention disease
    n1=xanthomatose cérébro-tendineuse | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=51
  65. xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:chylomicron retention disease
    n1=xanthomatose cérébrotendineuse | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=51
  66. acrodermatite entéropathique --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=acrodermatite entéropathique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  67. en:Tay-Sachs disease --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=en:Tay-Sachs disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  68. en:Wolman's disease --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=en:Wolman's disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  69. maladie de wolman --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=maladie de wolman | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  70. syndrome de dubin-johnson --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=syndrome de dubin-johnson | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  71. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  72. xérodermite pigmentaire --- r_associated #0: 50 --> en:chylomicron retention disease
    n1=xérodermite pigmentaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=50
  73. en:acrodermatitis enteropathica --- r_associated #0: 49 --> en:chylomicron retention disease
    n1=en:acrodermatitis enteropathica | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=49
  74. en:cerebrotendinous xanthomatosis --- r_associated #0: 48 --> en:chylomicron retention disease
    n1=en:cerebrotendinous xanthomatosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=48
  75. syndrome de Dubin-Johnson --- r_associated #0: 48 --> en:chylomicron retention disease
    n1=syndrome de Dubin-Johnson | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=48
  76. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 46 --> en:chylomicron retention disease
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=46
  77. en:dubin-johnson syndrome --- r_associated #0: 45 --> en:chylomicron retention disease
    n1=en:dubin-johnson syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=45
  78. mucolipidose type II --- r_associated #0: 45 --> en:chylomicron retention disease
    n1=mucolipidose type II | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=45
  79. mucolipidose type ii --- r_associated #0: 45 --> en:chylomicron retention disease
    n1=mucolipidose type ii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=45
  80. sirop d'érable (urine à odeur de) --- r_associated #0: 44 --> en:chylomicron retention disease
    n1=sirop d'érable (urine à odeur de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=44
  81. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  82. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  83. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  84. en:factor v and factor viii, combined deficiency of --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=en:factor v and factor viii, combined deficiency of | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  85. en:fountain syndrome --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=en:fountain syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  86. en:robinow-like syndrome --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=en:robinow-like syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  87. rétention placentaire --- r_associated #0: 43 --> en:chylomicron retention disease
    n1=rétention placentaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=43
  88. en:brain calcification rajab type --- r_associated #0: 42 --> en:chylomicron retention disease
    n1=en:brain calcification rajab type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=42
  89. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 42 --> en:chylomicron retention disease
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=42
  90. en:gamma-glutamyltransferase deficiency --- r_associated #0: 42 --> en:chylomicron retention disease
    n1=en:gamma-glutamyltransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=42
  91. en:muscle amp deaminase deficiency --- r_associated #0: 42 --> en:chylomicron retention disease
    n1=en:muscle amp deaminase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=42
  92. en:allgrove syndrome --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=en:allgrove syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  93. en:generalized peeling skin syndrome --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=en:generalized peeling skin syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  94. en:smith-mccort dysplasia --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=en:smith-mccort dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  95. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  96. hérédité autosomale récessive --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=hérédité autosomale récessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  97. v+ --- r_associated #0: 41 --> en:chylomicron retention disease
    n1=v+ | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=41
  98. V+ --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=V+ | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  99. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=Walker-Warburg (syndrome de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  100. déficit en céto-acide décarboxylase --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=déficit en céto-acide décarboxylase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  101. en:autosomal recessive inheritance --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:autosomal recessive inheritance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  102. en:autosomal recessive ocular albinism --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:autosomal recessive ocular albinism | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  103. en:classical maple syrup urine disease --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:classical maple syrup urine disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  104. en:congenital leptin deficiency --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:congenital leptin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  105. en:hereditary fructose intolerance --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:hereditary fructose intolerance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  106. en:maple syrup urine disease --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:maple syrup urine disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  107. en:persistent mullerian duct syndrome --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:persistent mullerian duct syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  108. en:placental retention --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:placental retention | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  109. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  110. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  111. intolérance au fructose --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=intolérance au fructose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  112. leucinose --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=leucinose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  113. maladie de Tay-sachs --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=maladie de Tay-sachs | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  114. maladie de tay-sachs --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=maladie de tay-sachs | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  115. maladie des urines avec odeur de sirop erable --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=maladie des urines avec odeur de sirop erable | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  116. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  117. maladie du sirop d'érable --- r_associated #0: 40 --> en:chylomicron retention disease
    n1=maladie du sirop d'érable | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=40
  118. en:biotinidase deficiency --- r_associated #0: 39 --> en:chylomicron retention disease
    n1=en:biotinidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=39
  119. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 39 --> en:chylomicron retention disease
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=39
  120. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 39 --> en:chylomicron retention disease
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=39
  121. en:glutamate-cysteine ligase deficiency --- r_associated #0: 38 --> en:chylomicron retention disease
    n1=en:glutamate-cysteine ligase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=38
  122. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 38 --> en:chylomicron retention disease
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=38
  123. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 38 --> en:chylomicron retention disease
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=38
  124. neuro-acanthocytose --- r_associated #0: 38 --> en:chylomicron retention disease
    n1=neuro-acanthocytose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=38
  125. en:hereditary factor xii deficiency disease --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:hereditary factor xii deficiency disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  126. en:hyperimmunoglobulin e syndrome --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:hyperimmunoglobulin e syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  127. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  128. en:pili torti onychodysplasia syndrome --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:pili torti onychodysplasia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  129. en:porphobilinogen synthase deficiency --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:porphobilinogen synthase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  130. en:senile dementia --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:senile dementia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  131. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  132. maladie de Niemann-Pick --- r_associated #0: 37 --> en:chylomicron retention disease
    n1=maladie de Niemann-Pick | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=37
  133. déficit en prolidase --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=déficit en prolidase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  134. en:hypophosphatasia infantile --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=en:hypophosphatasia infantile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  135. en:neuroacanthocytosis --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=en:neuroacanthocytosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  136. en:sar1b, ser179arg --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=en:sar1b, ser179arg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  137. en:tungland bellman syndrome --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=en:tungland bellman syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  138. en:warsaw breakage syndrome --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=en:warsaw breakage syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  139. histiocytose sinusale hémophagocytaire --- r_associated #0: 36 --> en:chylomicron retention disease
    n1=histiocytose sinusale hémophagocytaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=36
  140. Wolman (maladie de) --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=Wolman (maladie de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  141. en:21-hydroxylase deficiency --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:21-hydroxylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  142. en:Niemann-Pick disease --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:Niemann-Pick disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  143. en:alkaptonuria --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:alkaptonuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  144. en:alpha, alpha-trehalase deficiency --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:alpha, alpha-trehalase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  145. en:anauxetic dysplasia --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:anauxetic dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  146. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  147. en:argininosuccinic aciduria --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:argininosuccinic aciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  148. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  149. en:bothnia retinal dystrophy --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:bothnia retinal dystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  150. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  151. en:deafness and myopia syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:deafness and myopia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  152. en:deficiency of glucosyltransferase 1 --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:deficiency of glucosyltransferase 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  153. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  154. en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  155. en:isolated hyperchlorhidrosis --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:isolated hyperchlorhidrosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  156. en:isovaleric acidemia --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:isovaleric acidemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  157. en:jankovic rivera syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:jankovic rivera syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  158. en:knobloch syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:knobloch syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  159. en:microcephaly-capillary malformation syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  160. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  161. en:morm syndrome --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:morm syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  162. en:pelizaeus merzbacher like disease --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:pelizaeus merzbacher like disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  163. en:pseudocholinesterase deficiency --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:pseudocholinesterase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  164. en:sar1b, 349, g-c, -1 --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:sar1b, 349, g-c, -1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  165. en:severe early childhood onset retinal dystrophy --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=en:severe early childhood onset retinal dystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  166. hyperchylomicronémie --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=hyperchylomicronémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  167. maladie de Crigler-Najjar --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=maladie de Crigler-Najjar | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  168. rétentionniste --- r_associated #0: 35 --> en:chylomicron retention disease
    n1=rétentionniste | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  169. en:3-methylglutaconic aciduria type iv --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:3-methylglutaconic aciduria type iv | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  170. en:acrocallosal syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:acrocallosal syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  171. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  172. en:aminoacylase 1 deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:aminoacylase 1 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  173. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  174. en:argininemia --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:argininemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  175. en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  176. en:childhood hypophosphatasia (disorder) --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  177. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  178. en:corpus callosum agenesis neuronopathy --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:corpus callosum agenesis neuronopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  179. en:crisponi syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:crisponi syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  180. en:deafness, progressive, with stapes fixation --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:deafness, progressive, with stapes fixation | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  181. en:desmosterolosis --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:desmosterolosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  182. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  183. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  184. en:familial hypoaldosteronism --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:familial hypoaldosteronism | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  185. en:glycogen storage disease type i --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:glycogen storage disease type i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  186. en:glycogen storage disease type x --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:glycogen storage disease type x | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  187. en:gracile syndrome (disorder) --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:gracile syndrome (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  188. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  189. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  190. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  191. en:insulin growth factor i deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:insulin growth factor i deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  192. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  193. en:kallman syndrome with heart disease --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:kallman syndrome with heart disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  194. en:leucinosis --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:leucinosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  195. en:macular corneal dystrophy --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:macular corneal dystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  196. en:maroteaux-lamy syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:maroteaux-lamy syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  197. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  198. en:pelviscapular dysplasia --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:pelviscapular dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  199. en:propionic acidemia --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:propionic acidemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  200. en:pseudotrisomy 13 syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  201. en:sar1b, 4-bp dup, 555ttac --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:sar1b, 4-bp dup, 555ttac | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  202. en:split-hand/foot malformation 3 --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:split-hand/foot malformation 3 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  203. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  204. en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  205. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  206. en:verloes bourguignon syndrome --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=en:verloes bourguignon syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  207. rétention des chylomicrons (maladie de la) --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=rétention des chylomicrons (maladie de la) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  208. rétention hydrochlorurée sodique --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=rétention hydrochlorurée sodique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  209. syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 34 --> en:chylomicron retention disease
    n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  210. dysplasie craniodiaphysaire --- r_associated #0: 33 --> en:chylomicron retention disease
    n1=dysplasie craniodiaphysaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=33
  211. rétention placentaire du postabortum --- r_associated #0: 33 --> en:chylomicron retention disease
    n1=rétention placentaire du postabortum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=33
  212. en:absence of chylomicrons in lymph and plasma --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:absence of chylomicrons in lymph and plasma | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  213. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  214. en:al awadi syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:al awadi syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  215. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  216. en:aminomethyltransferase deficiency --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:aminomethyltransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  217. en:atrophoderma vermiculatum --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:atrophoderma vermiculatum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  218. en:bamforth syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:bamforth syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  219. en:bardet-biedl syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:bardet-biedl syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  220. en:behr syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:behr syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  221. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  222. en:chondrodysplasia punctata syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:chondrodysplasia punctata syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  223. en:congenital disorder of glycosylation type ig --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type ig | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  224. en:cooper jabs syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:cooper jabs syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  225. en:cryptophthalmos syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:cryptophthalmos syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  226. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  227. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  228. en:fronto-facio-nasal dysplasia --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:fronto-facio-nasal dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  229. en:hereditary factor xi deficiency disease --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:hereditary factor xi deficiency disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  230. en:hyperchylomicronaemia --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:hyperchylomicronaemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  231. en:hypomandibular faciocranial dysostosis --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:hypomandibular faciocranial dysostosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  232. en:laurence-moon syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:laurence-moon syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  233. en:lethal congenital contracture syndrome 1 --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:lethal congenital contracture syndrome 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  234. en:majeed syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:majeed syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  235. en:mannosidosis --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:mannosidosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  236. en:maple-tree syrup disease --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:maple-tree syrup disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  237. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  238. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  239. en:microcephaly, amish type (disorder) --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:microcephaly, amish type (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  240. en:north american indian childhood cirrhosis --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:north american indian childhood cirrhosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  241. en:odontohypophosphatasia (disorder) --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:odontohypophosphatasia (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  242. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  243. en:prolidase deficiency --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:prolidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  244. en:renal dysplasia - limb defects syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:renal dysplasia - limb defects syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  245. en:sarcosinemia --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:sarcosinemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  246. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  247. en:sly syndrome --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:sly syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  248. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  249. en:tyrosinemia, type iii --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:tyrosinemia, type iii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  250. en:werdnig-hoffmann disease --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:werdnig-hoffmann disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  251. en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 32 --> en:chylomicron retention disease
    n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=32
  252. déficit en neuraminidase --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=déficit en neuraminidase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  253. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  254. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  255. en:ataxia telangiectasia syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:ataxia telangiectasia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  256. en:ataxia with vitamin e deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:ataxia with vitamin e deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  257. en:brody myopathy --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:brody myopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  258. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  259. en:combined malonic and methylmalonic aciduria --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:combined malonic and methylmalonic aciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  260. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  261. en:congenital disorder of glycosylation type id --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type id | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  262. en:congenital disorder of glycosylation type ie --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type ie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  263. en:congenital disorder of glycosylation, type if --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation, type if | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  264. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  265. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  266. en:congenital transferrin deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:congenital transferrin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  267. en:diaphanospondylodysostosis --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:diaphanospondylodysostosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  268. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  269. en:ehlers-danlos syndrome, type vi --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:ehlers-danlos syndrome, type vi | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  270. en:enterokinase deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:enterokinase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  271. en:familial acantholysis --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:familial acantholysis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  272. en:familial renal iminoglycinuria --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:familial renal iminoglycinuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  273. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  274. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  275. en:hmg-coa lyase deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hmg-coa lyase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  276. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  277. en:hyperlipoproteinemia type i --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hyperlipoproteinemia type i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  278. en:hypokalemia, familial --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hypokalemia, familial | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  279. en:hypomagnesemia 1, intestinal --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:hypomagnesemia 1, intestinal | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  280. en:marles greenberg persaud syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:marles greenberg persaud syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  281. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  282. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  283. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  284. en:multiple sulfatase deficiency disease --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:multiple sulfatase deficiency disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  285. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  286. en:neuraminidase deficiency --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:neuraminidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  287. en:neutral lipid storage disease with myopathy --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:neutral lipid storage disease with myopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  288. en:peeling skin syndrome, acral type --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:peeling skin syndrome, acral type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  289. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  290. en:reardon hall slaney syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:reardon hall slaney syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  291. en:saito kuba tsuruta syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:saito kuba tsuruta syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  292. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  293. en:trichohepatoenteric syndrome --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:trichohepatoenteric syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  294. en:tyrosinemia type ii --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=en:tyrosinemia type ii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  295. fucosidose --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=fucosidose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  296. histidinémie --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=histidinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  297. mucolipidose II --- r_associated #0: 31 --> en:chylomicron retention disease
    n1=mucolipidose II | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=31
  298. abêtalipoprotéinémie normotriglycéridémique de type Steinberg --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=abêtalipoprotéinémie normotriglycéridémique de type Steinberg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  299. adénite sinusale cytophagique --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=adénite sinusale cytophagique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  300. démence (sémiologie) --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=démence (sémiologie) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  301. en:Dubin-Johnson's syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:Dubin-Johnson's syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  302. en:Leroy's i-cell disease --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:Leroy's i-cell disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  303. en:acrorenal mandibular syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:acrorenal mandibular syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  304. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  305. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  306. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  307. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  308. en:branched-chain ketoaciduria --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:branched-chain ketoaciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  309. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  310. en:cohen syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:cohen syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  311. en:congenital disorder of glycosylation type 1h --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type 1h | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  312. en:congenital disorder of glycosylation type ia --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type ia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  313. en:craniodiaphyseal dysplasia --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:craniodiaphyseal dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  314. en:donnai-barrow syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:donnai-barrow syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  315. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  316. en:familial median cleft of upper and lower lip --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:familial median cleft of upper and lower lip | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  317. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  318. en:fucosidosis --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:fucosidosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  319. en:hereditary factor x deficiency disease --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:hereditary factor x deficiency disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  320. en:hnsha due to aldolase a deficiency --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:hnsha due to aldolase a deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  321. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  322. en:hyperphosphatasia with mental retardation --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:hyperphosphatasia with mental retardation | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  323. en:hyperprolinemia type 1 --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:hyperprolinemia type 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  324. en:jejunal endoscopy shows white epithelium --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:jejunal endoscopy shows white epithelium | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  325. en:late-onset junctional epidermolysis bullosa --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:late-onset junctional epidermolysis bullosa | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  326. en:lethal congenital contracture syndrome 2 --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:lethal congenital contracture syndrome 2 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  327. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  328. en:membranous retention --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:membranous retention | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  329. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  330. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  331. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  332. en:mucopolysaccharidosis i --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:mucopolysaccharidosis i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  333. en:mucopolysaccharidosis type i --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:mucopolysaccharidosis type i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  334. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  335. en:netherton syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:netherton syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  336. en:niemann-pick disease --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:niemann-pick disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  337. en:oculocutaneous albinism type 6 --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:oculocutaneous albinism type 6 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  338. en:orotic aciduria --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:orotic aciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  339. en:otoonychoperoneal syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:otoonychoperoneal syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  340. en:papillon-lefevre syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:papillon-lefevre syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  341. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  342. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  343. en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  344. en:rapadilino syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:rapadilino syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  345. en:spondylo-ocular syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:spondylo-ocular syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  346. en:spondyloenchondrodysplasia --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:spondyloenchondrodysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  347. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  348. en:steatorrhea --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:steatorrhea | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  349. en:tetra-amelia autosomal recessive --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:tetra-amelia autosomal recessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  350. en:waardenburg anophthalmia syndrome --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=en:waardenburg anophthalmia syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  351. maladie de Tay-Sachs --- r_associated #0: 30 --> en:chylomicron retention disease
    n1=maladie de Tay-Sachs | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30
  352. en:Laurence-Moon's syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:Laurence-Moon's syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  353. en:acid phosphatase deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:acid phosphatase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  354. en:alpha-1 antitrypsin deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:alpha-1 antitrypsin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  355. en:autosomal recessive ichthyosis --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:autosomal recessive ichthyosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  356. en:cerebellar ataxia, cayman type --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:cerebellar ataxia, cayman type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  357. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  358. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  359. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  360. en:congenital disorder of glycosylation type 2e --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type 2e | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  361. en:defect in chylomicron secretion --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:defect in chylomicron secretion | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  362. en:ethanolaminosis --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:ethanolaminosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  363. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  364. en:glutamate formiminotransferase deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:glutamate formiminotransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  365. en:glutathione synthetase deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:glutathione synthetase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  366. en:histidinemia --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:histidinemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  367. en:hyperlipoproteinemia type I --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:hyperlipoproteinemia type I | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  368. en:hypomyelination and congenital cataract --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:hypomyelination and congenital cataract | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  369. en:jervell and lange nielsen syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:jervell and lange nielsen syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  370. en:kuskokwim disease --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:kuskokwim disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  371. en:lethal larsen-like syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:lethal larsen-like syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  372. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  373. en:macdermot winter syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:macdermot winter syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  374. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  375. en:morquio syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:morquio syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  376. en:n-acetylglutamate synthase deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:n-acetylglutamate synthase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  377. en:neonatal progeroid syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:neonatal progeroid syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  378. en:nonaka myopathy --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:nonaka myopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  379. en:northern epilepsy syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:northern epilepsy syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  380. en:retinitis punctata albescens (disorder) --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:retinitis punctata albescens (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  381. en:richards-rundle syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:richards-rundle syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  382. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  383. en:sanfilippo syndrome --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:sanfilippo syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  384. en:sar1b, gly185val --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:sar1b, gly185val | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  385. en:thyroid dyshormonogenesis 4 --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:thyroid dyshormonogenesis 4 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  386. en:transcobalamin ii deficiency --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=en:transcobalamin ii deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  387. mucopolysaccharidose de type I --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=mucopolysaccharidose de type I | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  388. rétention membraneuse --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=rétention membraneuse | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  389. rétention sudorale --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=rétention sudorale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  390. syndrome de Laurence-Moon --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=syndrome de Laurence-Moon | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  391. xanthique (lithiase) --- r_associated #0: 29 --> en:chylomicron retention disease
    n1=xanthique (lithiase) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=29
  392. Maladie de Wolman --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=Maladie de Wolman | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  393. déficit en sulfite-oxydase --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=déficit en sulfite-oxydase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  394. en:2-hydroxyglutaric aciduria --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:2-hydroxyglutaric aciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  395. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  396. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  397. en:adrenal gland hyperplasia ii --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:adrenal gland hyperplasia ii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  398. en:arterial tortuosity syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:arterial tortuosity syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  399. en:autosomal recessive scid --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:autosomal recessive scid | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  400. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  401. en:brown-vialetto-van laere syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:brown-vialetto-van laere syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  402. en:chitty hall baraitser syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:chitty hall baraitser syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  403. en:citrin deficiency --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:citrin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  404. en:congenital analbuminemia --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:congenital analbuminemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  405. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  406. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  407. en:decreased vibratory sense --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:decreased vibratory sense | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  408. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  409. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  410. en:fabry disease --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:fabry disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  411. en:geroderma osteodysplastica --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:geroderma osteodysplastica | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  412. en:growth retardation --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:growth retardation | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  413. en:heart defects limb shortening --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:heart defects limb shortening | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  414. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  415. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  416. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  417. en:hypospadias-mental retardation syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:hypospadias-mental retardation syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  418. en:kaufman-mckusick syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:kaufman-mckusick syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  419. en:lactase deficiency, congenital --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:lactase deficiency, congenital | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  420. en:manouvrier syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:manouvrier syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  421. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  422. en:najjar syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:najjar syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  423. en:nathalie syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:nathalie syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  424. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  425. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  426. en:phenylketonuria ii --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:phenylketonuria ii | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  427. en:prolonged electroretinal response suppression --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:prolonged electroretinal response suppression | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  428. en:sitosterolemia with xanthomatosis --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:sitosterolemia with xanthomatosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  429. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  430. en:sulfite oxidase deficiency --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:sulfite oxidase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  431. en:thomas syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:thomas syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  432. en:uv-sensitive syndrome --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:uv-sensitive syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  433. en:valinemia --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=en:valinemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  434. hyperglycéridémie mixte --- r_associated #0: 28 --> en:chylomicron retention disease
    n1=hyperglycéridémie mixte | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=28
  435. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  436. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  437. en:Bassen-Kornzweig disease --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:Bassen-Kornzweig disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  438. en:Bassen-Kornzweig's disease --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:Bassen-Kornzweig's disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  439. en:albinotic fundus --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:albinotic fundus | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  440. en:allanson pantzar mcleod syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:allanson pantzar mcleod syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  441. en:alpha-fetoprotein deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:alpha-fetoprotein deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  442. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  443. en:aspartylglycosaminuria --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:aspartylglycosaminuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  444. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  445. en:autosomal recessive primary microcephaly --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:autosomal recessive primary microcephaly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  446. en:behrens baumann dust syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:behrens baumann dust syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  447. en:bestrophinopathy, autosomal recessive --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:bestrophinopathy, autosomal recessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  448. en:beta-aminoisobutyricaciduria --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:beta-aminoisobutyricaciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  449. en:bowen-conradi syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:bowen-conradi syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  450. en:braddock syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:braddock syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  451. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  452. en:classical phenylketonuria --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:classical phenylketonuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  453. en:congenital bowing of long bone --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:congenital bowing of long bone | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  454. en:congenital disorder of glycosylation type ic --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:congenital disorder of glycosylation type ic | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  455. en:cutis laxa, autosomal recessive --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:cutis laxa, autosomal recessive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  456. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  457. en:deficiency of fat-soluble vitamins --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:deficiency of fat-soluble vitamins | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  458. en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  459. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  460. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  461. en:gurrieri sammito bellussi syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:gurrieri sammito bellussi syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  462. en:histidinaemia --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:histidinaemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  463. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  464. en:hyperprolinemia type 2 --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:hyperprolinemia type 2 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  465. en:infantile onset --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:infantile onset | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  466. en:isolated hypoplasia of the right ventricle --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:isolated hypoplasia of the right ventricle | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  467. en:laron syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:laron syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  468. en:leukotriene c4 synthase deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:leukotriene c4 synthase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  469. en:lipoidosis --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:lipoidosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  470. en:lipoprotein glomerulopathy --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:lipoprotein glomerulopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  471. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  472. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  473. en:peripheral nervous system disorder --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:peripheral nervous system disorder | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  474. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  475. en:sar1b, glu122ter --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:sar1b, glu122ter | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  476. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  477. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  478. en:type ii acrocephalopolysyndactyly --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:type ii acrocephalopolysyndactyly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  479. en:urocanase deficiency --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:urocanase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  480. en:xanthinuria, type i --- r_associated #0: 27 --> en:chylomicron retention disease
    n1=en:xanthinuria, type i | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=27
  481. Anderson --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=Anderson | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  482. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  483. en:5-oxoprolinase deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:5-oxoprolinase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  484. en:Crigler Najjar's disease --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:Crigler Najjar's disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  485. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  486. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  487. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  488. en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:autosomal recessive sideroblastic anemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  489. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  490. en:basal ganglia disease, biotin-responsive --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:basal ganglia disease, biotin-responsive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  491. en:becker generalized myotonia --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:becker generalized myotonia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  492. en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:charcot-marie-tooth disease type 4 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  493. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  494. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  495. en:craniofacial ulnar renal syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:craniofacial ulnar renal syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  496. en:crigler-najjar syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:crigler-najjar syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  497. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  498. en:deafness, sensorineural, and male infertility --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:deafness, sensorineural, and male infertility | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  499. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  500. en:dicarboxylicaminoaciduria --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:dicarboxylicaminoaciduria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  501. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  502. en:fryns macrocephaly --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:fryns macrocephaly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  503. en:hall riggs syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:hall riggs syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  504. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  505. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  506. en:infantile globoid cell leukodystrophy --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:infantile globoid cell leukodystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  507. en:isaacs syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:isaacs syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  508. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  509. en:malabsorption syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:malabsorption syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  510. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  511. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  512. en:moyamoya disease with early onset achalasia --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:moyamoya disease with early onset achalasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  513. en:naxos disease --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:naxos disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  514. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  515. en:neurologic deficits may occur secondarily to malabsorption --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:neurologic deficits may occur secondarily to malabsorption | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  516. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  517. en:oculocutaneous albinism type 4 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:oculocutaneous albinism type 4 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  518. en:presentey anomaly --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:presentey anomaly | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  519. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  520. en:pyle metaphyseal dysplasia --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:pyle metaphyseal dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  521. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  522. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  523. en:sar1b, 2-bp del, 75tg --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:sar1b, 2-bp del, 75tg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  524. en:sar1b, asp137asn --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:sar1b, asp137asn | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  525. en:sar1b, gly37arg --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:sar1b, gly37arg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  526. en:serum triglycerides normal --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:serum triglycerides normal | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  527. en:sonoda syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:sonoda syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  528. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  529. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  530. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  531. en:vomitus --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:vomitus | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  532. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  533. syndrome de malabsorption --- r_associated #0: 26 --> en:chylomicron retention disease
    n1=syndrome de malabsorption | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=26
  534. déficit congénital en mégacaryocytes --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=déficit congénital en mégacaryocytes | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  535. en:Dubin-Sprinz disease --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:Dubin-Sprinz disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  536. en:autosomal recessive asexual dwarfism --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:autosomal recessive asexual dwarfism | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  537. en:brachydactyly syndrome type b --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:brachydactyly syndrome type b | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  538. en:cystinosis --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:cystinosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  539. en:emesia --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:emesia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  540. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  541. en:intestinal epithelial dysplasia --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:intestinal epithelial dysplasia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  542. en:joubert syndrome --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:joubert syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  543. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  544. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 25 --> en:chylomicron retention disease
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25
  545. acrodermatitis enteropathica --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=acrodermatitis enteropathica | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  546. en:alstrom syndrome --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:alstrom syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  547. en:baller-gerold syndrome --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:baller-gerold syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  548. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  549. en:deficiency of fructokinase --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:deficiency of fructokinase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  550. en:hypocholesterolemia --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:hypocholesterolemia | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  551. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  552. en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  553. en:sweat retention --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=en:sweat retention | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  554. maladie de dubin-johnson --- r_associated #0: 24 --> en:chylomicron retention disease
    n1=maladie de dubin-johnson | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=24
  555. en:Laron syndrome --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:Laron syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  556. en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  557. en:emesis --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:emesis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  558. en:hepatolenticular degeneration --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:hepatolenticular degeneration | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  559. en:intestinal malabsorption of fat --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:intestinal malabsorption of fat | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  560. en:lecithin acyltransferase deficiency --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:lecithin acyltransferase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  561. en:oxalosis --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:oxalosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  562. en:pentosuria --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:pentosuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  563. en:small bowel enterocytes accumulate lipid droplets in membrane-bound compartments or in the cytoplasm --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:small bowel enterocytes accumulate lipid droplets in membrane-bound compartments or in the cytoplasm | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  564. en:type a 14 --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:type a 14 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  565. en:wolman's disease --- r_associated #0: 23 --> en:chylomicron retention disease
    n1=en:wolman's disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=23
  566. en:malnutrition --- r_associated #0: 22 --> en:chylomicron retention disease
    n1=en:malnutrition | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=22
  567. en:missed abortion --- r_associated #0: 22 --> en:chylomicron retention disease
    n1=en:missed abortion | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=22
  568. en:peters-plus syndrome --- r_associated #0: 22 --> en:chylomicron retention disease
    n1=en:peters-plus syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=22
  569. en:reduced tendon reflexes --- r_associated #0: 22 --> en:chylomicron retention disease
    n1=en:reduced tendon reflexes | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=22
  570. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 22 --> en:chylomicron retention disease
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=22
  571. Maladie de Tay-Sachs --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=Maladie de Tay-Sachs | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  572. acidurie argininosuccinique --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=acidurie argininosuccinique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  573. acidémie isovalérique --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=acidémie isovalérique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  574. alcaptonurie --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=alcaptonurie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  575. argininémie --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=argininémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  576. cétoacidurie à chaînes ramifiées --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=cétoacidurie à chaînes ramifiées | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  577. déficit en biotinidase --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=déficit en biotinidase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  578. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=déficit enzymatique partiel de la surrénale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  579. en:Nathalie syndrome --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:Nathalie syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  580. en:ear, patella, short stature syndrome --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:ear, patella, short stature syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  581. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  582. en:retained afterbirth --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:retained afterbirth | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  583. en:retentionist --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:retentionist | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  584. en:severe diarrhea --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:severe diarrhea | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  585. en:tyrosinemia type II --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:tyrosinemia type II | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  586. en:zinc-deficiency type --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=en:zinc-deficiency type | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  587. idiosyncrasie au fructose --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=idiosyncrasie au fructose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  588. mannosidose --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=mannosidose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  589. mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=mucopolysaccharidose de type 1 | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  590. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  591. syndrome de Zellweger --- r_associated #0: 21 --> en:chylomicron retention disease
    n1=syndrome de Zellweger | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  592. Anderson (maladie d') --- r_associated #0: 20 --> en:chylomicron retention disease
    n1=Anderson (maladie d') | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=20
  593. Sénilité --- r_associated #0: 20 --> en:chylomicron retention disease
    n1=Sénilité | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=20
  594. médecine --- r_associated #0: 20 --> en:chylomicron retention disease
    n1=médecine | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=20
  595. syndrome de Warburg --- r_associated #0: 16 --> en:chylomicron retention disease
    n1=syndrome de Warburg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=16
  596. Fuchs (syndrome de) --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Fuchs (syndrome de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  597. His (faisceau de) --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=His (faisceau de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  598. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Hyperplasie congénitale des surrénales | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  599. Intolérance au fructose --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Intolérance au fructose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  600. Maladie de Niemann-Pick --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Maladie de Niemann-Pick | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  601. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Syndrome de Walker-Warburg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  602. Vomissement --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=Vomissement | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  603. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:chylomicron retention disease
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=15
  604. hyperlipoprotéinémie de type I --- r_associated #0: 11 --> en:chylomicron retention disease
    n1=hyperlipoprotéinémie de type I | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=11
  605. A-bêta-lipoprotéinémie --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=A-bêta-lipoprotéinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  606. Aberfeld (syndrome d') --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Aberfeld (syndrome d') | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  607. Crigler-Najjar (maladie de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Crigler-Najjar (maladie de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  608. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Dubin-Johnson (syndrome de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  609. Fucosidose --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Fucosidose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  610. Histidinémie --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Histidinémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  611. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Laurence-Moon (syndrome de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  612. Manning (score de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Manning (score de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  613. Mannosidose --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Mannosidose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  614. Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Niemann-Pick (maladie de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  615. Retard de croissance --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Retard de croissance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  616. Sengstaken-Blakemore (sonde de) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Sengstaken-Blakemore (sonde de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  617. Syndrome de malabsorption --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Syndrome de malabsorption | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  618. VOMISSEMENTS --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=VOMISSEMENTS | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  619. Vomissements --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=Vomissements | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  620. alcalose métabolique (classification) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=alcalose métabolique (classification) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  621. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=cornée et tyrosinose de type II | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  622. démence d'Alzheimer --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence d'Alzheimer | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  623. démence frontotemporale --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence frontotemporale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  624. démence héréditaire et infarctus multiples cérébraux --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence héréditaire et infarctus multiples cérébraux | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  625. démence myoclonique --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence myoclonique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  626. démence parkinsonienne avec dégénérescence pallidopontonigrée --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence parkinsonienne avec dégénérescence pallidopontonigrée | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  627. démence précoce --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence précoce | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  628. démence pugilistique --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence pugilistique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  629. démence régressive --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence régressive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  630. démence sémantique --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=démence sémantique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  631. en:HHH syndrome --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:HHH syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  632. en:Tay Sachs' disease --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:Tay Sachs' disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  633. en:alcaptonuria --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:alcaptonuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  634. en:homogentisuria --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:homogentisuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  635. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  636. en:intestinal malabsorption --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:intestinal malabsorption | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  637. en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:phosphatide thesaurismosis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  638. en:retained placenta --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:retained placenta | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  639. en:xanthine lithiasis --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=en:xanthine lithiasis | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  640. maladie de Bassen-Kornzweig --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=maladie de Bassen-Kornzweig | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  641. maladie de niemann-pick --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=maladie de niemann-pick | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  642. maladie du système nerveux périphérique --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=maladie du système nerveux périphérique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  643. malnutrition --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=malnutrition | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  644. nanisme de type Laron --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=nanisme de type Laron | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  645. neuraminidase (déficit en) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=neuraminidase (déficit en) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  646. prolidase (déficit en) --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=prolidase (déficit en) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  647. sirtuine --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=sirtuine | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  648. sisi-test --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=sisi-test | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  649. sismothérapie --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=sismothérapie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  650. syndrome de Nathalie --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=syndrome de Nathalie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  651. syndrome de warburg --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=syndrome de warburg | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  652. syndrome de zellweger --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=syndrome de zellweger | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  653. xanthomatose familiale primitive --- r_associated #0: 10 --> en:chylomicron retention disease
    n1=xanthomatose familiale primitive | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=10
  654. Rétention placentaire --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=Rétention placentaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  655. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=Tay-Sachs (maladie de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  656. affection nerveuse périphérique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=affection nerveuse périphérique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  657. démence alcoolique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence alcoolique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  658. démence aluminique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence aluminique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  659. démence sous-corticale --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence sous-corticale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  660. démence sénile de type Alzheimer --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence sénile de type Alzheimer | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  661. démence sénile mixte --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence sénile mixte | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  662. démence traumatique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence traumatique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  663. démence vasculaire --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence vasculaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  664. démence vésanique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence vésanique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  665. démence à corps de Lewy --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démence à corps de Lewy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  666. démences et prions --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=démences et prions | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  667. en:Sachs' disease --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=en:Sachs' disease | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  668. en:peripheral neuropathy --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=en:peripheral neuropathy | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  669. faisceau de His --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=faisceau de His | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  670. fuchsine --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=fuchsine | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  671. fucose --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=fucose | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  672. fucosidase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=fucosidase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  673. fucoside --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=fucoside | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  674. histaminergie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminergie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  675. histaminergique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminergique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  676. histaminique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  677. histaminolibération --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminolibération | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  678. histaminolytique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminolytique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  679. histaminopexie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminopexie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  680. histaminurie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminurie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  681. histaminémie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histaminémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  682. histidase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  683. histidinase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidinase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  684. histidine --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidine | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  685. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidine-ammoniac-lyase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  686. histidine-décarboxylase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidine-décarboxylase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  687. histidine-désaminase --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=histidine-désaminase | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  688. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=hyperostose vertébrale ankylosante | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  689. hyperoxalurie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=hyperoxalurie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  690. hyperoxalémie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=hyperoxalémie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  691. malabsorption (syndrome de) --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=malabsorption (syndrome de) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  692. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  693. neuropathie périphérique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=neuropathie périphérique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  694. semidominance --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=semidominance | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  695. semiquinone --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=semiquinone | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  696. syndrome de Fuchs --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=syndrome de Fuchs | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  697. séminal --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminal | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  698. séminifère --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminifère | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  699. séminomateux --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminomateux | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  700. séminome --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  701. séminome de l'ovaire --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminome de l'ovaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  702. séminome du médiastin --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminome du médiastin | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  703. séminome spermatocytaire --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=séminome spermatocytaire | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  704. sémiochimique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=sémiochimique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  705. sémiologie extrapyramidale --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=sémiologie extrapyramidale | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  706. trouble nerveux périphérique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=trouble nerveux périphérique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  707. vomitus --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=vomitus | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  708. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthoastrocytome pléomorphe | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  709. xanthochromie --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthochromie | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  710. xanthochromie caroténique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthochromie caroténique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  711. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthoerythrodermia perstans | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  712. xanthogranulome juvénile --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthogranulome juvénile | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  713. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthogranulome nécrobiotique | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  714. xanthogranulome palpébral --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthogranulome palpébral | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  715. xanthohistiocytome --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthohistiocytome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  716. xanthoma disseminatum --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthoma disseminatum | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=5
  717. xanthomatose --- r_associated #0: 5 --> en:chylomicron retention disease
    n1=xanthomatose | n2=en:chylomicron retention disease | 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