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'en:epstein syndrome (disorder)'
(id=6897328 ; fe=en:epstein syndrome (disorder) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=4019 creation date=2017-06-25 touchdate=2025-08-21 11:43:18.000)
≈ 114 relations sortantes

  1. en:epstein syndrome (disorder) -- r_associated #0: 41 / 1 -> en:chronic focal glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic focal glomerulonephritis | rel=r_associated | relid=0 | w=41
  2. en:epstein syndrome (disorder) -- r_associated #0: 35 / 0.854 -> en:benign granulocytopenia in childhood
    n1=en:epstein syndrome (disorder) | n2=en:benign granulocytopenia in childhood | rel=r_associated | relid=0 | w=35
  3. en:epstein syndrome (disorder) -- r_associated #0: 35 / 0.854 -> en:chronic hypoplastic neutropenia
    n1=en:epstein syndrome (disorder) | n2=en:chronic hypoplastic neutropenia | rel=r_associated | relid=0 | w=35
  4. en:epstein syndrome (disorder) -- r_associated #0: 35 / 0.854 -> en:encounter due to personal history of nephrotic syndrome
    n1=en:epstein syndrome (disorder) | n2=en:encounter due to personal history of nephrotic syndrome | rel=r_associated | relid=0 | w=35
  5. en:epstein syndrome (disorder) -- r_associated #0: 35 / 0.854 -> en:fanconi anemia
    n1=en:epstein syndrome (disorder) | n2=en:fanconi anemia | rel=r_associated | relid=0 | w=35
  6. en:epstein syndrome (disorder) -- r_associated #0: 35 / 0.854 -> en:idiopathic thrombocytopenic purpura
    n1=en:epstein syndrome (disorder) | n2=en:idiopathic thrombocytopenic purpura | rel=r_associated | relid=0 | w=35
  7. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:autosomal dominant inheritance
    n1=en:epstein syndrome (disorder) | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=34
  8. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:chronic rapidly progressive glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic rapidly progressive glomerulonephritis | rel=r_associated | relid=0 | w=34
  9. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:hereditary spherocytosis due to beta spectrin defect
    n1=en:epstein syndrome (disorder) | n2=en:hereditary spherocytosis due to beta spectrin defect | rel=r_associated | relid=0 | w=34
  10. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:hereditary spherocytosis due to spectrin deficiency
    n1=en:epstein syndrome (disorder) | n2=en:hereditary spherocytosis due to spectrin deficiency | rel=r_associated | relid=0 | w=34
  11. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:membranous glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:membranous glomerulonephritis | rel=r_associated | relid=0 | w=34
  12. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> en:thin membrane nephropathy
    n1=en:epstein syndrome (disorder) | n2=en:thin membrane nephropathy | rel=r_associated | relid=0 | w=34
  13. en:epstein syndrome (disorder) -- r_associated #0: 34 / 0.829 -> Epstein
    n1=en:epstein syndrome (disorder) | n2=Epstein | rel=r_associated | relid=0 | w=34
  14. en:epstein syndrome (disorder) -- r_associated #0: 32 / 0.78 -> en:chronic glomerulonephritis with other specified pathological lesion in kidney
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis with other specified pathological lesion in kidney | rel=r_associated | relid=0 | w=32
  15. en:epstein syndrome (disorder) -- r_associated #0: 32 / 0.78 -> en:chronic nephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic nephritis | rel=r_associated | relid=0 | w=32
  16. en:epstein syndrome (disorder) -- r_associated #0: 32 / 0.78 -> en:disorder of hematopoietic system in newborn
    n1=en:epstein syndrome (disorder) | n2=en:disorder of hematopoietic system in newborn | rel=r_associated | relid=0 | w=32
  17. en:epstein syndrome (disorder) -- r_associated #0: 32 / 0.78 -> en:hemolytic anemia due to hyperbaric oxygen
    n1=en:epstein syndrome (disorder) | n2=en:hemolytic anemia due to hyperbaric oxygen | rel=r_associated | relid=0 | w=32
  18. en:epstein syndrome (disorder) -- r_associated #0: 32 / 0.78 -> en:primary myelofibrosis
    n1=en:epstein syndrome (disorder) | n2=en:primary myelofibrosis | rel=r_associated | relid=0 | w=32
  19. en:epstein syndrome (disorder) -- r_associated #0: 31 / 0.756 -> en:congenital anomaly of the hematopoietic system
    n1=en:epstein syndrome (disorder) | n2=en:congenital anomaly of the hematopoietic system | rel=r_associated | relid=0 | w=31
  20. en:epstein syndrome (disorder) -- r_associated #0: 31 / 0.756 -> en:sebastian syndrome
    n1=en:epstein syndrome (disorder) | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=31
  21. en:epstein syndrome (disorder) -- r_associated #0: 30 / 0.732 -> en:hematopoietic and lymphoid cell neoplasm
    n1=en:epstein syndrome (disorder) | n2=en:hematopoietic and lymphoid cell neoplasm | rel=r_associated | relid=0 | w=30
  22. en:epstein syndrome (disorder) -- r_associated #0: 30 / 0.732 -> en:hereditary diffuse mesangiocapillary glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:hereditary diffuse mesangiocapillary glomerulonephritis | rel=r_associated | relid=0 | w=30
  23. en:epstein syndrome (disorder) -- r_associated #0: 30 / 0.732 -> en:hyperfiltration focal segmental glomerulosclerosis
    n1=en:epstein syndrome (disorder) | n2=en:hyperfiltration focal segmental glomerulosclerosis | rel=r_associated | relid=0 | w=30
  24. en:epstein syndrome (disorder) -- r_associated #0: 30 / 0.732 -> en:montreal platelet syndrome
    n1=en:epstein syndrome (disorder) | n2=en:montreal platelet syndrome | rel=r_associated | relid=0 | w=30
  25. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:chronic glomerulonephritis associated with another disorder
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis associated with another disorder | rel=r_associated | relid=0 | w=29
  26. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:chronic proliferative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic proliferative glomerulonephritis | rel=r_associated | relid=0 | w=29
  27. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:familial hemophagocytic lymphohistiocytosis
    n1=en:epstein syndrome (disorder) | n2=en:familial hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=29
  28. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:hereditary diffuse membranous glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:hereditary diffuse membranous glomerulonephritis | rel=r_associated | relid=0 | w=29
  29. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:may-hegglin anomaly
    n1=en:epstein syndrome (disorder) | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=29
  30. en:epstein syndrome (disorder) -- r_associated #0: 29 / 0.707 -> en:renal failure, progressive, with hypertension
    n1=en:epstein syndrome (disorder) | n2=en:renal failure, progressive, with hypertension | rel=r_associated | relid=0 | w=29
  31. en:epstein syndrome (disorder) -- r_associated #0: 28 / 0.683 -> en:albinism co-occurrent with hematologic disorder
    n1=en:epstein syndrome (disorder) | n2=en:albinism co-occurrent with hematologic disorder | rel=r_associated | relid=0 | w=28
  32. en:epstein syndrome (disorder) -- r_associated #0: 28 / 0.683 -> en:alport syndrome-like hereditary nephritis
    n1=en:epstein syndrome (disorder) | n2=en:alport syndrome-like hereditary nephritis | rel=r_associated | relid=0 | w=28
  33. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:chronic diffuse glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic diffuse glomerulonephritis | rel=r_associated | relid=0 | w=27
  34. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:chronic exudative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic exudative glomerulonephritis | rel=r_associated | relid=0 | w=27
  35. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:chronic glomerulonephritis with lesion of membranous glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis with lesion of membranous glomerulonephritis | rel=r_associated | relid=0 | w=27
  36. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:chronic glomerulonephritis with lesion of proliferative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis with lesion of proliferative glomerulonephritis | rel=r_associated | relid=0 | w=27
  37. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:chronic nephritic syndrome, dense deposit disease
    n1=en:epstein syndrome (disorder) | n2=en:chronic nephritic syndrome, dense deposit disease | rel=r_associated | relid=0 | w=27
  38. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:end stage renal disease (33% of patients)
    n1=en:epstein syndrome (disorder) | n2=en:end stage renal disease (33% of patients) | rel=r_associated | relid=0 | w=27
  39. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> en:hemophagocytic lymphohistiocytosis
    n1=en:epstein syndrome (disorder) | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=27
  40. en:epstein syndrome (disorder) -- r_associated #0: 27 / 0.659 -> syndrome
    n1=en:epstein syndrome (disorder) | n2=syndrome | rel=r_associated | relid=0 | w=27
  41. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:bone marrow disorder
    n1=en:epstein syndrome (disorder) | n2=en:bone marrow disorder | rel=r_associated | relid=0 | w=26
  42. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:chronic
    n1=en:epstein syndrome (disorder) | n2=en:chronic | rel=r_associated | relid=0 | w=26
  43. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:chronic glomerulonephritis in diseases classified elsewhere
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis in diseases classified elsewhere | rel=r_associated | relid=0 | w=26
  44. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:chronic inflammation
    n1=en:epstein syndrome (disorder) | n2=en:chronic inflammation | rel=r_associated | relid=0 | w=26
  45. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:chronic nephritic syndrome, focal and segmental glomerular lesions
    n1=en:epstein syndrome (disorder) | n2=en:chronic nephritic syndrome, focal and segmental glomerular lesions | rel=r_associated | relid=0 | w=26
  46. en:epstein syndrome (disorder) -- r_associated #0: 26 / 0.634 -> en:sickle cell-thalassemia disease
    n1=en:epstein syndrome (disorder) | n2=en:sickle cell-thalassemia disease | rel=r_associated | relid=0 | w=26
  47. en:epstein syndrome (disorder) -- r_associated #0: 25 / 0.61 -> en:deafness, bilateral sensorineural, high frequency (100% of patients)
    n1=en:epstein syndrome (disorder) | n2=en:deafness, bilateral sensorineural, high frequency (100% of patients) | rel=r_associated | relid=0 | w=25
  48. en:epstein syndrome (disorder) -- r_associated #0: 25 / 0.61 -> en:epstein
    n1=en:epstein syndrome (disorder) | n2=en:epstein | rel=r_associated | relid=0 | w=25
  49. en:epstein syndrome (disorder) -- r_associated #0: 25 / 0.61 -> en:fechtner syndrome (disorder)
    n1=en:epstein syndrome (disorder) | n2=en:fechtner syndrome (disorder) | rel=r_associated | relid=0 | w=25
  50. en:epstein syndrome (disorder) -- r_associated #0: 24 / 0.585 -> en:microscopic hematuria
    n1=en:epstein syndrome (disorder) | n2=en:microscopic hematuria | rel=r_associated | relid=0 | w=24
  51. en:epstein syndrome (disorder) -- r_associated #0: 23 / 0.561 -> en:wiskott-aldrich syndrome
    n1=en:epstein syndrome (disorder) | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=23
  52. en:epstein syndrome (disorder) -- r_associated #0: 22 / 0.537 -> en:hematopoietic system disease associated with aids
    n1=en:epstein syndrome (disorder) | n2=en:hematopoietic system disease associated with aids | rel=r_associated | relid=0 | w=22
  53. en:epstein syndrome (disorder) -- r_associated #0: 22 / 0.537 -> en:nephritis
    n1=en:epstein syndrome (disorder) | n2=en:nephritis | rel=r_associated | relid=0 | w=22
  54. en:epstein syndrome (disorder) -- r_associated #0: 21 / 0.512 -> en:hereditary spherocytosis due to deficiency of protein 4.2
    n1=en:epstein syndrome (disorder) | n2=en:hereditary spherocytosis due to deficiency of protein 4.2 | rel=r_associated | relid=0 | w=21
  55. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> coeur triatrial
    n1=en:epstein syndrome (disorder) | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  56. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:10p13-p14 deletion syndrome
    n1=en:epstein syndrome (disorder) | n2=en:10p13-p14 deletion syndrome | rel=r_associated | relid=0 | w=20
  57. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:acrodysostosis 1
    n1=en:epstein syndrome (disorder) | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  58. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:epstein syndrome (disorder) | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  59. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:autoimmune polyglandular syndrome
    n1=en:epstein syndrome (disorder) | n2=en:autoimmune polyglandular syndrome | rel=r_associated | relid=0 | w=20
  60. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:bernard-soulier syndrome
    n1=en:epstein syndrome (disorder) | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=20
  61. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:carbonic anhydrase i deficiency
    n1=en:epstein syndrome (disorder) | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  62. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:cataract (alport syndrome with macrothrombocytopenia)
    n1=en:epstein syndrome (disorder) | n2=en:cataract (alport syndrome with macrothrombocytopenia) | rel=r_associated | relid=0 | w=20
  63. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:chromosome 16p12.1 deletion syndrome
    n1=en:epstein syndrome (disorder) | n2=en:chromosome 16p12.1 deletion syndrome | rel=r_associated | relid=0 | w=20
  64. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis | rel=r_associated | relid=0 | w=20
  65. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:chronic glomerulonephritis with unspecified pathological lesion in kidney
    n1=en:epstein syndrome (disorder) | n2=en:chronic glomerulonephritis with unspecified pathological lesion in kidney | rel=r_associated | relid=0 | w=20
  66. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:congenital dysmegakaryopoietic thrombocytopenia, paris trousseau type
    n1=en:epstein syndrome (disorder) | n2=en:congenital dysmegakaryopoietic thrombocytopenia, paris trousseau type | rel=r_associated | relid=0 | w=20
  67. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:cor triatriatum
    n1=en:epstein syndrome (disorder) | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  68. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:epstein syndrome (disorder) | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  69. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:epstein syndrome (disorder) | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20
  70. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:eiken type chondrodysplasia
    n1=en:epstein syndrome (disorder) | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  71. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:familial interstitial nephritis
    n1=en:epstein syndrome (disorder) | n2=en:familial interstitial nephritis | rel=r_associated | relid=0 | w=20
  72. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:giant platelet
    n1=en:epstein syndrome (disorder) | n2=en:giant platelet | rel=r_associated | relid=0 | w=20
  73. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:hereditary diffuse endocapillary proliferative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:hereditary diffuse endocapillary proliferative glomerulonephritis | rel=r_associated | relid=0 | w=20
  74. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:hereditary diffuse mesangial proliferative glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:hereditary diffuse mesangial proliferative glomerulonephritis | rel=r_associated | relid=0 | w=20
  75. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type iii
    n1=en:epstein syndrome (disorder) | n2=en:hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type iii | rel=r_associated | relid=0 | w=20
  76. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:hypertension, moderate, secondary to renal disease
    n1=en:epstein syndrome (disorder) | n2=en:hypertension, moderate, secondary to renal disease | rel=r_associated | relid=0 | w=20
  77. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:insulin receptor mutation - associated insulin resistance syndromes
    n1=en:epstein syndrome (disorder) | n2=en:insulin receptor mutation - associated insulin resistance syndromes | rel=r_associated | relid=0 | w=20
  78. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:kenny-caffey syndrome type 2
    n1=en:epstein syndrome (disorder) | n2=en:kenny-caffey syndrome type 2 | rel=r_associated | relid=0 | w=20
  79. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:epstein syndrome (disorder) | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  80. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:epstein syndrome (disorder) | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  81. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:maternal diabetes and deafness syndrome
    n1=en:epstein syndrome (disorder) | n2=en:maternal diabetes and deafness syndrome | rel=r_associated | relid=0 | w=20
  82. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mediterranean thrombocytopenia
    n1=en:epstein syndrome (disorder) | n2=en:mediterranean thrombocytopenia | rel=r_associated | relid=0 | w=20
  83. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mental retardation, autosomal dominant 9
    n1=en:epstein syndrome (disorder) | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  84. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mental retardation, autosomal recessive 34
    n1=en:epstein syndrome (disorder) | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  85. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:epstein syndrome (disorder) | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  86. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mild bleeding episodes (epistaxis, gi bleeding, menorrhagia)
    n1=en:epstein syndrome (disorder) | n2=en:mild bleeding episodes (epistaxis, gi bleeding, menorrhagia) | rel=r_associated | relid=0 | w=20
  87. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:minimal change glomerulonephritis
    n1=en:epstein syndrome (disorder) | n2=en:minimal change glomerulonephritis | rel=r_associated | relid=0 | w=20
  88. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mitochondrial dna depletion syndrome 12
    n1=en:epstein syndrome (disorder) | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  89. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mucolipidosis type iii gamma
    n1=en:epstein syndrome (disorder) | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  90. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:mullerian-renal-cervical spine syndrome
    n1=en:epstein syndrome (disorder) | n2=en:mullerian-renal-cervical spine syndrome | rel=r_associated | relid=0 | w=20
  91. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:multiple vascular disruption syndrome
    n1=en:epstein syndrome (disorder) | n2=en:multiple vascular disruption syndrome | rel=r_associated | relid=0 | w=20
  92. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:myh9-positive inclusions on immunohistochemical staining
    n1=en:epstein syndrome (disorder) | n2=en:myh9-positive inclusions on immunohistochemical staining | rel=r_associated | relid=0 | w=20
  93. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:myh9, arg702cys
    n1=en:epstein syndrome (disorder) | n2=en:myh9, arg702cys | rel=r_associated | relid=0 | w=20
  94. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:myh9, arg702his
    n1=en:epstein syndrome (disorder) | n2=en:myh9, arg702his | rel=r_associated | relid=0 | w=20
  95. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:no cataract (epstein syndrome)
    n1=en:epstein syndrome (disorder) | n2=en:no cataract (epstein syndrome) | rel=r_associated | relid=0 | w=20
  96. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:periodontitis co-occurrent with hematologic disorder
    n1=en:epstein syndrome (disorder) | n2=en:periodontitis co-occurrent with hematologic disorder | rel=r_associated | relid=0 | w=20
  97. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:plasma kallikrein deficiency
    n1=en:epstein syndrome (disorder) | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  98. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:platelet abnormality
    n1=en:epstein syndrome (disorder) | n2=en:platelet abnormality | rel=r_associated | relid=0 | w=20
  99. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:single central incisor syndrome
    n1=en:epstein syndrome (disorder) | n2=en:single central incisor syndrome | rel=r_associated | relid=0 | w=20
  100. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:thrombocytopenia
    n1=en:epstein syndrome (disorder) | n2=en:thrombocytopenia | rel=r_associated | relid=0 | w=20
  101. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:thrombopeny
    n1=en:epstein syndrome (disorder) | n2=en:thrombopeny | rel=r_associated | relid=0 | w=20
  102. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:tissue kallikrein deficiency
    n1=en:epstein syndrome (disorder) | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  103. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:triple a syndrome
    n1=en:epstein syndrome (disorder) | n2=en:triple a syndrome | rel=r_associated | relid=0 | w=20
  104. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:Triple a syndrome
    n1=en:epstein syndrome (disorder) | n2=en:Triple a syndrome | rel=r_associated | relid=0 | w=20
  105. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> en:wilms tumor 1 gene syndromes
    n1=en:epstein syndrome (disorder) | n2=en:wilms tumor 1 gene syndromes | rel=r_associated | relid=0 | w=20
  106. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> glomérulonéphrite extra-membraneuse
    n1=en:epstein syndrome (disorder) | n2=glomérulonéphrite extra-membraneuse | rel=r_associated | relid=0 | w=20
  107. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> glomérulonéphrite extramembraneuse
    n1=en:epstein syndrome (disorder) | n2=glomérulonéphrite extramembraneuse | rel=r_associated | relid=0 | w=20
  108. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> hématurie microscopique
    n1=en:epstein syndrome (disorder) | n2=hématurie microscopique | rel=r_associated | relid=0 | w=20
  109. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> inflammation chronique
    n1=en:epstein syndrome (disorder) | n2=inflammation chronique | rel=r_associated | relid=0 | w=20
  110. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> myélofibrose primaire
    n1=en:epstein syndrome (disorder) | n2=myélofibrose primaire | rel=r_associated | relid=0 | w=20
  111. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> myélofibrose primitive
    n1=en:epstein syndrome (disorder) | n2=myélofibrose primitive | rel=r_associated | relid=0 | w=20
  112. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> néphrite
    n1=en:epstein syndrome (disorder) | n2=néphrite | rel=r_associated | relid=0 | w=20
  113. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> thrombocytopénie
    n1=en:epstein syndrome (disorder) | n2=thrombocytopénie | rel=r_associated | relid=0 | w=20
  114. en:epstein syndrome (disorder) -- r_associated #0: 20 / 0.488 -> thrombopénie
    n1=en:epstein syndrome (disorder) | n2=thrombopénie | rel=r_associated | relid=0 | w=20
≈ 121 relations entrantes

  1. myélofibrose primaire --- r_associated #0: 125 --> en:epstein syndrome (disorder)
    n1=myélofibrose primaire | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=125
  2. myélofibrose primitive --- r_associated #0: 121 --> en:epstein syndrome (disorder)
    n1=myélofibrose primitive | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=121
  3. en:primary myelofibrosis --- r_associated #0: 118 --> en:epstein syndrome (disorder)
    n1=en:primary myelofibrosis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=118
  4. néphrite --- r_associated #0: 79 --> en:epstein syndrome (disorder)
    n1=néphrite | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=79
  5. en:nephritis --- r_associated #0: 77 --> en:epstein syndrome (disorder)
    n1=en:nephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=77
  6. cœur triatrial --- r_associated #0: 50 --> en:epstein syndrome (disorder)
    n1=cœur triatrial | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=50
  7. coeur triatrial --- r_associated #0: 47 --> en:epstein syndrome (disorder)
    n1=coeur triatrial | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=47
  8. glomérulonéphrite extramembraneuse --- r_associated #0: 44 --> en:epstein syndrome (disorder)
    n1=glomérulonéphrite extramembraneuse | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=44
  9. en:Triple a syndrome --- r_associated #0: 43 --> en:epstein syndrome (disorder)
    n1=en:Triple a syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=43
  10. Epstein --- r_associated #0: 42 --> en:epstein syndrome (disorder)
    n1=Epstein | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=42
  11. en:single central incisor syndrome --- r_associated #0: 42 --> en:epstein syndrome (disorder)
    n1=en:single central incisor syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=42
  12. en:thrombocytopenia --- r_associated #0: 42 --> en:epstein syndrome (disorder)
    n1=en:thrombocytopenia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=42
  13. glomérulonéphrite extra-membraneuse --- r_associated #0: 40 --> en:epstein syndrome (disorder)
    n1=glomérulonéphrite extra-membraneuse | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=40
  14. en:chronic rapidly progressive glomerulonephritis --- r_associated #0: 39 --> en:epstein syndrome (disorder)
    n1=en:chronic rapidly progressive glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=39
  15. en:myh9, arg702cys --- r_associated #0: 39 --> en:epstein syndrome (disorder)
    n1=en:myh9, arg702cys | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=39
  16. en:triple a syndrome --- r_associated #0: 39 --> en:epstein syndrome (disorder)
    n1=en:triple a syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=39
  17. en:platelet abnormality --- r_associated #0: 38 --> en:epstein syndrome (disorder)
    n1=en:platelet abnormality | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=38
  18. thrombocytopénie --- r_associated #0: 38 --> en:epstein syndrome (disorder)
    n1=thrombocytopénie | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=38
  19. thrombopénie --- r_associated #0: 38 --> en:epstein syndrome (disorder)
    n1=thrombopénie | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=38
  20. inflammation chronique --- r_associated #0: 37 --> en:epstein syndrome (disorder)
    n1=inflammation chronique | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=37
  21. en:hypertension, moderate, secondary to renal disease --- r_associated #0: 36 --> en:epstein syndrome (disorder)
    n1=en:hypertension, moderate, secondary to renal disease | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=36
  22. en:mediterranean thrombocytopenia --- r_associated #0: 36 --> en:epstein syndrome (disorder)
    n1=en:mediterranean thrombocytopenia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=36
  23. en:acrodysostosis 1 --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:acrodysostosis 1 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  24. en:chronic --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:chronic | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  25. en:chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  26. en:chronic glomerulonephritis with unspecified pathological lesion in kidney --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis with unspecified pathological lesion in kidney | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  27. en:familial hemophagocytic lymphohistiocytosis --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:familial hemophagocytic lymphohistiocytosis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  28. en:hematopoietic system disease associated with aids --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:hematopoietic system disease associated with aids | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  29. en:hemolytic anemia due to hyperbaric oxygen --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:hemolytic anemia due to hyperbaric oxygen | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  30. en:hereditary diffuse endocapillary proliferative glomerulonephritis --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:hereditary diffuse endocapillary proliferative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  31. en:hereditary diffuse membranous glomerulonephritis --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:hereditary diffuse membranous glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  32. en:kenny-caffey syndrome type 2 --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:kenny-caffey syndrome type 2 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  33. en:sebastian syndrome --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:sebastian syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  34. en:tissue kallikrein deficiency --- r_associated #0: 35 --> en:epstein syndrome (disorder)
    n1=en:tissue kallikrein deficiency | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=35
  35. en:benign granulocytopenia in childhood --- r_associated #0: 34 --> en:epstein syndrome (disorder)
    n1=en:benign granulocytopenia in childhood | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=34
  36. en:chronic nephritic syndrome, dense deposit disease --- r_associated #0: 34 --> en:epstein syndrome (disorder)
    n1=en:chronic nephritic syndrome, dense deposit disease | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=34
  37. en:fanconi anemia --- r_associated #0: 34 --> en:epstein syndrome (disorder)
    n1=en:fanconi anemia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=34
  38. en:fechtner syndrome (disorder) --- r_associated #0: 34 --> en:epstein syndrome (disorder)
    n1=en:fechtner syndrome (disorder) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=34
  39. en:wiskott-aldrich syndrome --- r_associated #0: 34 --> en:epstein syndrome (disorder)
    n1=en:wiskott-aldrich syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=34
  40. en:chronic inflammation --- r_associated #0: 33 --> en:epstein syndrome (disorder)
    n1=en:chronic inflammation | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=33
  41. en:alport syndrome-like hereditary nephritis --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:alport syndrome-like hereditary nephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  42. en:chronic glomerulonephritis with lesion of membranous glomerulonephritis --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis with lesion of membranous glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  43. en:chronic proliferative glomerulonephritis --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:chronic proliferative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  44. en:hereditary diffuse mesangial proliferative glomerulonephritis --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:hereditary diffuse mesangial proliferative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  45. en:hereditary spherocytosis due to deficiency of protein 4.2 --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:hereditary spherocytosis due to deficiency of protein 4.2 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  46. en:hyperfiltration focal segmental glomerulosclerosis --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:hyperfiltration focal segmental glomerulosclerosis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  47. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  48. en:multiple vascular disruption syndrome --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:multiple vascular disruption syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  49. en:periodontitis co-occurrent with hematologic disorder --- r_associated #0: 32 --> en:epstein syndrome (disorder)
    n1=en:periodontitis co-occurrent with hematologic disorder | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=32
  50. en:autoimmune polyglandular syndrome --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:autoimmune polyglandular syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  51. en:carbonic anhydrase i deficiency --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:carbonic anhydrase i deficiency | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  52. en:cataract (alport syndrome with macrothrombocytopenia) --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:cataract (alport syndrome with macrothrombocytopenia) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  53. en:chronic diffuse glomerulonephritis --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:chronic diffuse glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  54. en:chronic glomerulonephritis associated with another disorder --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis associated with another disorder | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  55. en:congenital dysmegakaryopoietic thrombocytopenia, paris trousseau type --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:congenital dysmegakaryopoietic thrombocytopenia, paris trousseau type | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  56. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  57. en:end stage renal disease (33% of patients) --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:end stage renal disease (33% of patients) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  58. en:familial interstitial nephritis --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:familial interstitial nephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  59. en:hematopoietic and lymphoid cell neoplasm --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:hematopoietic and lymphoid cell neoplasm | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  60. en:maternal diabetes and deafness syndrome --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:maternal diabetes and deafness syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  61. en:membranous glomerulonephritis --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:membranous glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  62. en:minimal change glomerulonephritis --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:minimal change glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  63. en:mullerian-renal-cervical spine syndrome --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=en:mullerian-renal-cervical spine syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  64. hématurie microscopique --- r_associated #0: 31 --> en:epstein syndrome (disorder)
    n1=hématurie microscopique | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=31
  65. en:autosomal dominant inheritance --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:autosomal dominant inheritance | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  66. en:bernard-soulier syndrome --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:bernard-soulier syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  67. en:chronic exudative glomerulonephritis --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:chronic exudative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  68. en:chronic glomerulonephritis with lesion of proliferative glomerulonephritis --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis with lesion of proliferative glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  69. en:chronic nephritic syndrome, focal and segmental glomerular lesions --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:chronic nephritic syndrome, focal and segmental glomerular lesions | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  70. en:microscopic hematuria --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:microscopic hematuria | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  71. en:mucolipidosis type iii gamma --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:mucolipidosis type iii gamma | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  72. en:plasma kallikrein deficiency --- r_associated #0: 30 --> en:epstein syndrome (disorder)
    n1=en:plasma kallikrein deficiency | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=30
  73. en:chromosome 16p12.1 deletion syndrome --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:chromosome 16p12.1 deletion syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  74. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  75. en:giant platelet --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:giant platelet | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  76. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  77. en:may-hegglin anomaly --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:may-hegglin anomaly | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  78. en:myh9, arg702his --- r_associated #0: 29 --> en:epstein syndrome (disorder)
    n1=en:myh9, arg702his | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=29
  79. en:albinism co-occurrent with hematologic disorder --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:albinism co-occurrent with hematologic disorder | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  80. en:bone marrow disorder --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:bone marrow disorder | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  81. en:chronic glomerulonephritis in diseases classified elsewhere --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis in diseases classified elsewhere | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  82. en:disorder of hematopoietic system in newborn --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:disorder of hematopoietic system in newborn | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  83. en:eiken type chondrodysplasia --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:eiken type chondrodysplasia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  84. en:hereditary diffuse mesangiocapillary glomerulonephritis --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:hereditary diffuse mesangiocapillary glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  85. en:hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type iii --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type iii | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  86. en:mental retardation, autosomal dominant 9 --- r_associated #0: 28 --> en:epstein syndrome (disorder)
    n1=en:mental retardation, autosomal dominant 9 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=28
  87. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  88. en:chronic glomerulonephritis with other specified pathological lesion in kidney --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:chronic glomerulonephritis with other specified pathological lesion in kidney | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  89. en:chronic nephritis --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:chronic nephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  90. en:cor triatriatum --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:cor triatriatum | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  91. en:deafness, bilateral sensorineural, high frequency (100% of patients) --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:deafness, bilateral sensorineural, high frequency (100% of patients) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  92. en:insulin receptor mutation - associated insulin resistance syndromes --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:insulin receptor mutation - associated insulin resistance syndromes | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  93. en:mental retardation, autosomal recessive 34 --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:mental retardation, autosomal recessive 34 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  94. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  95. en:mild bleeding episodes (epistaxis, gi bleeding, menorrhagia) --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:mild bleeding episodes (epistaxis, gi bleeding, menorrhagia) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  96. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  97. en:montreal platelet syndrome --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:montreal platelet syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  98. en:renal failure, progressive, with hypertension --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:renal failure, progressive, with hypertension | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  99. en:wilms tumor 1 gene syndromes --- r_associated #0: 27 --> en:epstein syndrome (disorder)
    n1=en:wilms tumor 1 gene syndromes | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=27
  100. en:10p13-p14 deletion syndrome --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:10p13-p14 deletion syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  101. en:encounter due to personal history of nephrotic syndrome --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:encounter due to personal history of nephrotic syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  102. en:hereditary spherocytosis due to beta spectrin defect --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:hereditary spherocytosis due to beta spectrin defect | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  103. en:myh9-positive inclusions on immunohistochemical staining --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:myh9-positive inclusions on immunohistochemical staining | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  104. en:no cataract (epstein syndrome) --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:no cataract (epstein syndrome) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  105. en:thrombopeny --- r_associated #0: 26 --> en:epstein syndrome (disorder)
    n1=en:thrombopeny | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=26
  106. en:thrombopenia --- r_associated #0: 23 --> en:epstein syndrome (disorder)
    n1=en:thrombopenia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=23
  107. Thrombopénie --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=Thrombopénie | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  108. en:chronic focal glomerulonephritis --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:chronic focal glomerulonephritis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  109. en:chronic hypoplastic neutropenia --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:chronic hypoplastic neutropenia | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  110. en:congenital anomaly of the hematopoietic system --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:congenital anomaly of the hematopoietic system | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  111. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:hemophagocytic lymphohistiocytosis | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  112. en:hereditary spherocytosis due to spectrin deficiency --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:hereditary spherocytosis due to spectrin deficiency | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  113. en:idiopathic thrombocytopenic purpura --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:idiopathic thrombocytopenic purpura | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  114. en:sickle cell-thalassemia disease --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:sickle cell-thalassemia disease | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  115. en:thin membrane nephropathy --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=en:thin membrane nephropathy | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  116. syndrome --- r_associated #0: 20 --> en:epstein syndrome (disorder)
    n1=syndrome | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=20
  117. Inflammation chronique --- r_associated #0: 10 --> en:epstein syndrome (disorder)
    n1=Inflammation chronique | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=10
  118. Thrombocytopénie --- r_associated #0: 10 --> en:epstein syndrome (disorder)
    n1=Thrombocytopénie | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=10
  119. thrombolytique (traitement) --- r_associated #0: 10 --> en:epstein syndrome (disorder)
    n1=thrombolytique (traitement) | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=10
  120. inflammation (protéine de l') --- r_associated #0: 5 --> en:epstein syndrome (disorder)
    n1=inflammation (protéine de l') | n2=en:epstein syndrome (disorder) | rel=r_associated | relid=0 | w=5
  121. syndromes du gène 1 de la tumeur de Wilms --- r_associated #0: 5 --> en:epstein syndrome (disorder)
    n1=syndromes du gène 1 de la tumeur de Wilms | n2=en:epstein syndrome (disorder) | 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