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'en:deafness, autosomal recessive 1a'
(id=6833760 ; fe=en:deafness, autosomal recessive 1a ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=50056 creation date=2017-06-25 touchdate=2025-08-14 00:15:45.000)
≈ 908 relations sortantes

  1. en:deafness, autosomal recessive 1a -- r_associated #0: 43 / 1 -> en:autosomal recessive hypohidrotic ectodermal dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=43
  2. en:deafness, autosomal recessive 1a -- r_associated #0: 42 / 0.977 -> en:liddle syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=42
  3. en:deafness, autosomal recessive 1a -- r_associated #0: 42 / 0.977 -> en:low frequency hearing loss
    n1=en:deafness, autosomal recessive 1a | n2=en:low frequency hearing loss | rel=r_associated | relid=0 | w=42
  4. en:deafness, autosomal recessive 1a -- r_associated #0: 42 / 0.977 -> en:malignant atrophic papulosis
    n1=en:deafness, autosomal recessive 1a | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=42
  5. en:deafness, autosomal recessive 1a -- r_associated #0: 42 / 0.977 -> en:mullerian inhibiting factor deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=42
  6. en:deafness, autosomal recessive 1a -- r_associated #0: 42 / 0.977 -> en:tracheobronchomalacia
    n1=en:deafness, autosomal recessive 1a | n2=en:tracheobronchomalacia | rel=r_associated | relid=0 | w=42
  7. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:cytochrome-c oxidase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=41
  8. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:gjb2, val84met
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, val84met | rel=r_associated | relid=0 | w=41
  9. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:kimura disease
    n1=en:deafness, autosomal recessive 1a | n2=en:kimura disease | rel=r_associated | relid=0 | w=41
  10. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:lissencephaly
    n1=en:deafness, autosomal recessive 1a | n2=en:lissencephaly | rel=r_associated | relid=0 | w=41
  11. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:pelger-huet anomaly
    n1=en:deafness, autosomal recessive 1a | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=41
  12. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:seckel syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=41
  13. en:deafness, autosomal recessive 1a -- r_associated #0: 41 / 0.953 -> en:simpson golabi behmel syndrome type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=41
  14. en:deafness, autosomal recessive 1a -- r_associated #0: 40 / 0.93 -> en:lysosomal storage disease
    n1=en:deafness, autosomal recessive 1a | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=40
  15. en:deafness, autosomal recessive 1a -- r_associated #0: 40 / 0.93 -> en:muenke syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=40
  16. en:deafness, autosomal recessive 1a -- r_associated #0: 40 / 0.93 -> en:ossification of posterior longitudinal ligament
    n1=en:deafness, autosomal recessive 1a | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=40
  17. en:deafness, autosomal recessive 1a -- r_associated #0: 40 / 0.93 -> en:porphyria cutanea tarda
    n1=en:deafness, autosomal recessive 1a | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=40
  18. en:deafness, autosomal recessive 1a -- r_associated #0: 39 / 0.907 -> en:dextrocardia
    n1=en:deafness, autosomal recessive 1a | n2=en:dextrocardia | rel=r_associated | relid=0 | w=39
  19. en:deafness, autosomal recessive 1a -- r_associated #0: 39 / 0.907 -> en:gynatresia
    n1=en:deafness, autosomal recessive 1a | n2=en:gynatresia | rel=r_associated | relid=0 | w=39
  20. en:deafness, autosomal recessive 1a -- r_associated #0: 39 / 0.907 -> en:progressive muscular atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:progressive muscular atrophy | rel=r_associated | relid=0 | w=39
  21. en:deafness, autosomal recessive 1a -- r_associated #0: 39 / 0.907 -> en:usher syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:usher syndrome | rel=r_associated | relid=0 | w=39
  22. en:deafness, autosomal recessive 1a -- r_associated #0: 38 / 0.884 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=38
  23. en:deafness, autosomal recessive 1a -- r_associated #0: 38 / 0.884 -> en:syringomyelia
    n1=en:deafness, autosomal recessive 1a | n2=en:syringomyelia | rel=r_associated | relid=0 | w=38
  24. en:deafness, autosomal recessive 1a -- r_associated #0: 38 / 0.884 -> en:waterhouse-friderichsen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=38
  25. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:acatalasemia
    n1=en:deafness, autosomal recessive 1a | n2=en:acatalasemia | rel=r_associated | relid=0 | w=37
  26. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:deafness, autosomal recessive 1a | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=37
  27. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:arnold-chiari malformation
    n1=en:deafness, autosomal recessive 1a | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=37
  28. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:hallermann syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=37
  29. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:mevalonate kinase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:mevalonate kinase deficiency | rel=r_associated | relid=0 | w=37
  30. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:rett syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:rett syndrome | rel=r_associated | relid=0 | w=37
  31. en:deafness, autosomal recessive 1a -- r_associated #0: 37 / 0.86 -> en:treacher collins syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=37
  32. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=36
  33. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:cerebrotendinous xanthomatosis
    n1=en:deafness, autosomal recessive 1a | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=36
  34. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:erythromelalgia
    n1=en:deafness, autosomal recessive 1a | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=36
  35. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:fryns syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=36
  36. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:hearing loss
    n1=en:deafness, autosomal recessive 1a | n2=en:hearing loss | rel=r_associated | relid=0 | w=36
  37. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:olivopontocerebellar atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=36
  38. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:pierre robin syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=36
  39. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:popliteal pterygium syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=36
  40. en:deafness, autosomal recessive 1a -- r_associated #0: 36 / 0.837 -> en:stiff person syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=36
  41. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:17q21 microdeletion syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=35
  42. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:aagenaes syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=35
  43. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:abetalipoproteinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=35
  44. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:achromatopsia
    n1=en:deafness, autosomal recessive 1a | n2=en:achromatopsia | rel=r_associated | relid=0 | w=35
  45. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:acrocallosal syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=35
  46. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:acrodermatitis
    n1=en:deafness, autosomal recessive 1a | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=35
  47. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=35
  48. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=35
  49. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:amniotic band syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=35
  50. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:aortic coarctation
    n1=en:deafness, autosomal recessive 1a | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=35
  51. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:arthrogryposis
    n1=en:deafness, autosomal recessive 1a | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=35
  52. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:beta-methylcrotonylglycinuria
    n1=en:deafness, autosomal recessive 1a | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=35
  53. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:brown-sequard syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=35
  54. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:cadasil syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=35
  55. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:campomelic dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=35
  56. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011)
    n1=en:deafness, autosomal recessive 1a | n2=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) | rel=r_associated | relid=0 | w=35
  57. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35
  58. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:congenital bilateral aplasia of the vas deferens
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=35
  59. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:craniosynostosis
    n1=en:deafness, autosomal recessive 1a | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=35
  60. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:ellis-van creveld syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=35
  61. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:epidermolysis bullosa
    n1=en:deafness, autosomal recessive 1a | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=35
  62. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:factor v leiden
    n1=en:deafness, autosomal recessive 1a | n2=en:factor v leiden | rel=r_associated | relid=0 | w=35
  63. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:familial mediterranean fever
    n1=en:deafness, autosomal recessive 1a | n2=en:familial mediterranean fever | rel=r_associated | relid=0 | w=35
  64. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:familial periodic paralysis
    n1=en:deafness, autosomal recessive 1a | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=35
  65. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:fetal akinesia deformation sequence
    n1=en:deafness, autosomal recessive 1a | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=35
  66. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:gjb2, 12-bp del, 1-bp ins, nt51
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 12-bp del, 1-bp ins, nt51 | rel=r_associated | relid=0 | w=35
  67. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:gjb2, arg143gln
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, arg143gln | rel=r_associated | relid=0 | w=35
  68. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:hemochromatosis
    n1=en:deafness, autosomal recessive 1a | n2=en:hemochromatosis | rel=r_associated | relid=0 | w=35
  69. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:jervell and lange nielsen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=35
  70. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:kearns-sayre syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=35
  71. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:kleine-levin syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=35
  72. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:kshv inflammatory cytokine syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=35
  73. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:leber hereditary optic atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=35
  74. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:leigh disease
    n1=en:deafness, autosomal recessive 1a | n2=en:leigh disease | rel=r_associated | relid=0 | w=35
  75. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:loeys-dietz syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=35
  76. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=35
  77. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:meckel-gruber syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=35
  78. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=35
  79. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:melkersson-rosenthal syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=35
  80. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:meningeal tuberculosis
    n1=en:deafness, autosomal recessive 1a | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=35
  81. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:menkes disease
    n1=en:deafness, autosomal recessive 1a | n2=en:menkes disease | rel=r_associated | relid=0 | w=35
  82. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:mmih syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
  83. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:myhre syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=35
  84. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:n-acetylglutamate synthase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=35
  85. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:neuroacanthocytosis
    n1=en:deafness, autosomal recessive 1a | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=35
  86. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:oeis complex
    n1=en:deafness, autosomal recessive 1a | n2=en:oeis complex | rel=r_associated | relid=0 | w=35
  87. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:orofacial cleft 1
    n1=en:deafness, autosomal recessive 1a | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=35
  88. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:osteopoikilosis
    n1=en:deafness, autosomal recessive 1a | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=35
  89. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:pain agnosia
    n1=en:deafness, autosomal recessive 1a | n2=en:pain agnosia | rel=r_associated | relid=0 | w=35
  90. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:panuveitis
    n1=en:deafness, autosomal recessive 1a | n2=en:panuveitis | rel=r_associated | relid=0 | w=35
  91. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:perthes disease
    n1=en:deafness, autosomal recessive 1a | n2=en:perthes disease | rel=r_associated | relid=0 | w=35
  92. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:pyruvate carboxylase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=35
  93. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:radial aplasia-thrombocytopenia syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=35
  94. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:roberts syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  95. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:sensorineural hearing loss
    n1=en:deafness, autosomal recessive 1a | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=35
  96. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:shprintzen-goldberg craniosynostosis syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=35
  97. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:stiff skin syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:stiff skin syndrome | rel=r_associated | relid=0 | w=35
  98. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:synpolydactyly
    n1=en:deafness, autosomal recessive 1a | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=35
  99. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:thyroid hormone resistance syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=35
  100. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:trisomy 14 mosaicism
    n1=en:deafness, autosomal recessive 1a | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=35
  101. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:variegate porphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=35
  102. en:deafness, autosomal recessive 1a -- r_associated #0: 35 / 0.814 -> en:x-linked dominant hypophosphatemic rickets
    n1=en:deafness, autosomal recessive 1a | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=35
  103. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:about half of patients report vestibular symptoms
    n1=en:deafness, autosomal recessive 1a | n2=en:about half of patients report vestibular symptoms | rel=r_associated | relid=0 | w=34
  104. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:acrodermatitis enteropathica
    n1=en:deafness, autosomal recessive 1a | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=34
  105. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:alkaptonuria
    n1=en:deafness, autosomal recessive 1a | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=34
  106. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:atransferrinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=34
  107. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:bilateral deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:bilateral deafness | rel=r_associated | relid=0 | w=34
  108. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:chorea
    n1=en:deafness, autosomal recessive 1a | n2=en:chorea | rel=r_associated | relid=0 | w=34
  109. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:chromosome 2q37 deletion syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=34
  110. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:complete deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:complete deafness | rel=r_associated | relid=0 | w=34
  111. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:congenital structural myopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=34
  112. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:cryptophthalmos syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=34
  113. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:deafness, autosomal recessive 1a (disorder)
    n1=en:deafness, autosomal recessive 1a | n2=en:deafness, autosomal recessive 1a (disorder) | rel=r_associated | relid=0 | w=34
  114. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  115. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:dyschromatosis symmetrica hereditaria
    n1=en:deafness, autosomal recessive 1a | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=34
  116. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:fuchs endothelial dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:fuchs endothelial dystrophy | rel=r_associated | relid=0 | w=34
  117. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:gjb2, 1-bp del, 167t
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 1-bp del, 167t | rel=r_associated | relid=0 | w=34
  118. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:glycogen storage disease
    n1=en:deafness, autosomal recessive 1a | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=34
  119. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:hellp syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=34
  120. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:hereditary hyperbilirubinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=34
  121. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:hyperpipecolatemia
    n1=en:deafness, autosomal recessive 1a | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=34
  122. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:leopard syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=34
  123. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:machado-joseph disease
    n1=en:deafness, autosomal recessive 1a | n2=en:machado-joseph disease | rel=r_associated | relid=0 | w=34
  124. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:malformations of cortical development
    n1=en:deafness, autosomal recessive 1a | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=34
  125. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:marburg virus disease
    n1=en:deafness, autosomal recessive 1a | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=34
  126. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:marfan syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=34
  127. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:melas syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:melas syndrome | rel=r_associated | relid=0 | w=34
  128. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:mitochondrial neurogastrointestingal encephalopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=34
  129. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:mixed connective tissue disease
    n1=en:deafness, autosomal recessive 1a | n2=en:mixed connective tissue disease | rel=r_associated | relid=0 | w=34
  130. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:mulibrey nanism
    n1=en:deafness, autosomal recessive 1a | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=34
  131. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:neonatal progeroid syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=34
  132. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:neurocysticercosis
    n1=en:deafness, autosomal recessive 1a | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=34
  133. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:ochronosis
    n1=en:deafness, autosomal recessive 1a | n2=en:ochronosis | rel=r_associated | relid=0 | w=34
  134. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:optic neuritis
    n1=en:deafness, autosomal recessive 1a | n2=en:optic neuritis | rel=r_associated | relid=0 | w=34
  135. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:pinta
    n1=en:deafness, autosomal recessive 1a | n2=en:pinta | rel=r_associated | relid=0 | w=34
  136. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:pityriasis rubra pilaris
    n1=en:deafness, autosomal recessive 1a | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=34
  137. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:plague
    n1=en:deafness, autosomal recessive 1a | n2=en:plague | rel=r_associated | relid=0 | w=34
  138. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:primary progressive aphasia
    n1=en:deafness, autosomal recessive 1a | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=34
  139. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:pseudoxanthoma elasticum
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudoxanthoma elasticum | rel=r_associated | relid=0 | w=34
  140. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:pulmonary alveolar proteinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=34
  141. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:rhizomelic dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=34
  142. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:robinow syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=34
  143. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:scimitar syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=34
  144. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:staphylococcal scalded skin syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=34
  145. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:swyer james syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=34
  146. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:thrombocytopenia 2
    n1=en:deafness, autosomal recessive 1a | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=34
  147. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:urea cycle metabolism disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=34
  148. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:wandering spleen
    n1=en:deafness, autosomal recessive 1a | n2=en:wandering spleen | rel=r_associated | relid=0 | w=34
  149. en:deafness, autosomal recessive 1a -- r_associated #0: 34 / 0.791 -> en:xerophthalmia
    n1=en:deafness, autosomal recessive 1a | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=34
  150. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:achard syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:achard syndrome | rel=r_associated | relid=0 | w=32
  151. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:agnosia
    n1=en:deafness, autosomal recessive 1a | n2=en:agnosia | rel=r_associated | relid=0 | w=32
  152. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:albinism
    n1=en:deafness, autosomal recessive 1a | n2=en:albinism | rel=r_associated | relid=0 | w=32
  153. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:albright's hereditary osteodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=32
  154. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:aprosencephaly
    n1=en:deafness, autosomal recessive 1a | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=32
  155. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:auditory perceptual disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=32
  156. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=32
  157. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:benign mucous membrane pemphigoid
    n1=en:deafness, autosomal recessive 1a | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=32
  158. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:berardinelli-seip congenital lipodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=32
  159. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004)
    n1=en:deafness, autosomal recessive 1a | n2=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) | rel=r_associated | relid=0 | w=32
  160. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002)
    n1=en:deafness, autosomal recessive 1a | n2=en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) | rel=r_associated | relid=0 | w=32
  161. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:complex regional pain syndrome ii
    n1=en:deafness, autosomal recessive 1a | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=32
  162. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:congenital fiber-type disproportion
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=32
  163. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:cutis laxa
    n1=en:deafness, autosomal recessive 1a | n2=en:cutis laxa | rel=r_associated | relid=0 | w=32
  164. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:deaf-blind disorders
    n1=en:deafness, autosomal recessive 1a | n2=en:deaf-blind disorders | rel=r_associated | relid=0 | w=32
  165. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:diffuse cerebral sclerosis of schilder
    n1=en:deafness, autosomal recessive 1a | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=32
  166. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:dyggve-melchior-clausen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=32
  167. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:ebstein anomaly
    n1=en:deafness, autosomal recessive 1a | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=32
  168. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:ectromelia
    n1=en:deafness, autosomal recessive 1a | n2=en:ectromelia | rel=r_associated | relid=0 | w=32
  169. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:familial juvenile nephronophthisis
    n1=en:deafness, autosomal recessive 1a | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=32
  170. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:fatal familial insomnia
    n1=en:deafness, autosomal recessive 1a | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=32
  171. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:felty syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:felty syndrome | rel=r_associated | relid=0 | w=32
  172. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:fragile x syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=32
  173. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:gastroschisis
    n1=en:deafness, autosomal recessive 1a | n2=en:gastroschisis | rel=r_associated | relid=0 | w=32
  174. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:gjb2, glu118del
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, glu118del | rel=r_associated | relid=0 | w=32
  175. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:gjb2, trp77arg
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, trp77arg | rel=r_associated | relid=0 | w=32
  176. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:gjb2, val84leu
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, val84leu | rel=r_associated | relid=0 | w=32
  177. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:goodpasture syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=32
  178. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:hemophagocytic lymphohistiocytosis
    n1=en:deafness, autosomal recessive 1a | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=32
  179. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:hereditary orotic aciduria
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=32
  180. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:hermansky-pudlak syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=32
  181. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:holoprosencephaly
    n1=en:deafness, autosomal recessive 1a | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=32
  182. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:hyperkalemic periodic paralysis
    n1=en:deafness, autosomal recessive 1a | n2=en:hyperkalemic periodic paralysis | rel=r_associated | relid=0 | w=32
  183. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:jackson-weiss syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=32
  184. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:kabuki syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=32
  185. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:korsakoff syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=32
  186. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:lateral medullary syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=32
  187. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:leprosy
    n1=en:deafness, autosomal recessive 1a | n2=en:leprosy | rel=r_associated | relid=0 | w=32
  188. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:leptospirosis
    n1=en:deafness, autosomal recessive 1a | n2=en:leptospirosis | rel=r_associated | relid=0 | w=32
  189. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:malignant hyperthermia syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=32
  190. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:maple syrup urine disease
    n1=en:deafness, autosomal recessive 1a | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=32
  191. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:merrf syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=32
  192. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:neuromyelitis optica
    n1=en:deafness, autosomal recessive 1a | n2=en:neuromyelitis optica | rel=r_associated | relid=0 | w=32
  193. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:non-trisomic autosomal aneuploidy
    n1=en:deafness, autosomal recessive 1a | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=32
  194. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:osteochondrodysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=32
  195. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:pettigrew syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=32
  196. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:pick's disease
    n1=en:deafness, autosomal recessive 1a | n2=en:pick's disease | rel=r_associated | relid=0 | w=32
  197. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:plummer-vinson syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=32
  198. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:potocki-lupski syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=32
  199. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:primary carnitine deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=32
  200. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:pseudohypoaldosteronism
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudohypoaldosteronism | rel=r_associated | relid=0 | w=32
  201. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:retinoschisis
    n1=en:deafness, autosomal recessive 1a | n2=en:retinoschisis | rel=r_associated | relid=0 | w=32
  202. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:subacute sclerosing panencephalitis
    n1=en:deafness, autosomal recessive 1a | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=32
  203. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:sunct syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=32
  204. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:tay-sachs disease
    n1=en:deafness, autosomal recessive 1a | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=32
  205. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:trichothiodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=32
  206. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:van der woude syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=32
  207. en:deafness, autosomal recessive 1a -- r_associated #0: 32 / 0.744 -> en:weaver syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=32
  208. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:adiposis dolorosa
    n1=en:deafness, autosomal recessive 1a | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=31
  209. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:aniridia
    n1=en:deafness, autosomal recessive 1a | n2=en:aniridia | rel=r_associated | relid=0 | w=31
  210. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:carnosinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:carnosinemia | rel=r_associated | relid=0 | w=31
  211. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:cartilage hair hypoplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=31
  212. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:cat-eye syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=31
  213. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:charge syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:charge syndrome | rel=r_associated | relid=0 | w=31
  214. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:codas syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:codas syndrome | rel=r_associated | relid=0 | w=31
  215. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:coffin-lowry syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=31
  216. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:congenital dyserythropoietic anemia
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=31
  217. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:familial partial lipodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=31
  218. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:focal dermal hypoplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=31
  219. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:fox-fordyce disease
    n1=en:deafness, autosomal recessive 1a | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=31
  220. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:giant axonal neuropathy
    n1=en:deafness, autosomal recessive 1a | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=31
  221. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:gjb2, 1-bp del, 235c
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 1-bp del, 235c | rel=r_associated | relid=0 | w=31
  222. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:gjb2, leu90pro
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, leu90pro | rel=r_associated | relid=0 | w=31
  223. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:gjb2, trp24ter
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, trp24ter | rel=r_associated | relid=0 | w=31
  224. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:glycine encephalopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=31
  225. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:gray platelet syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=31
  226. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:heterotaxy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=31
  227. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:hydrops fetalis
    n1=en:deafness, autosomal recessive 1a | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=31
  228. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:hyperlysinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=31
  229. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=31
  230. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:idiopathic cd4-positive t-lymphocytopenia
    n1=en:deafness, autosomal recessive 1a | n2=en:idiopathic cd4-positive t-lymphocytopenia | rel=r_associated | relid=0 | w=31
  231. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:infantile neuroaxonal dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=31
  232. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:jacobsen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=31
  233. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:leri-weill dyschondrosteosis
    n1=en:deafness, autosomal recessive 1a | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=31
  234. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:deafness, autosomal recessive 1a | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=31
  235. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:multicentric osteolysis, nodulosis, and arthropathy
    n1=en:deafness, autosomal recessive 1a | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=31
  236. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  237. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:myotonic disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=31
  238. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:nadh dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:nadh dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  239. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:nail-patella syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=31
  240. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:orofaciodigital syndrome type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=31
  241. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:papillon-lefevre syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=31
  242. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:paragonimiasis
    n1=en:deafness, autosomal recessive 1a | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=31
  243. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:pearson marrow-pancreas syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=31
  244. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:prekallikrein deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:prekallikrein deficiency | rel=r_associated | relid=0 | w=31
  245. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:proteus syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=31
  246. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:scleredema adultorum
    n1=en:deafness, autosomal recessive 1a | n2=en:scleredema adultorum | rel=r_associated | relid=0 | w=31
  247. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:smith-magenis syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=31
  248. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:stargardt disease
    n1=en:deafness, autosomal recessive 1a | n2=en:stargardt disease | rel=r_associated | relid=0 | w=31
  249. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:transient global amnesia
    n1=en:deafness, autosomal recessive 1a | n2=en:transient global amnesia | rel=r_associated | relid=0 | w=31
  250. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:triploidy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=31
  251. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  252. en:deafness, autosomal recessive 1a -- r_associated #0: 31 / 0.721 -> en:xxxy and xxxxy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=31
  253. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:acquired hyperostosis syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=30
  254. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:acromegaly
    n1=en:deafness, autosomal recessive 1a | n2=en:acromegaly | rel=r_associated | relid=0 | w=30
  255. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:acute intermittent porphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=30
  256. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:allgrove syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=30
  257. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:arakawa syndrome ii
    n1=en:deafness, autosomal recessive 1a | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=30
  258. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:argininemia
    n1=en:deafness, autosomal recessive 1a | n2=en:argininemia | rel=r_associated | relid=0 | w=30
  259. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:argininosuccinic aciduria
    n1=en:deafness, autosomal recessive 1a | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=30
  260. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:autosomal dominant optic atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=30
  261. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:biotinidase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=30
  262. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:carnitine palmitoyltransferase ii deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=30
  263. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:choroideremia
    n1=en:deafness, autosomal recessive 1a | n2=en:choroideremia | rel=r_associated | relid=0 | w=30
  264. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:cogan-reese syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=30
  265. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=30
  266. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:congenital disorder of deglycosylation
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=30
  267. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:congenital insensitivity to pain with anhidrosis
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=30
  268. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:congenital pain insensitivity
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=30
  269. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:craniofacial dysostosis
    n1=en:deafness, autosomal recessive 1a | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=30
  270. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:cystathioninuria
    n1=en:deafness, autosomal recessive 1a | n2=en:cystathioninuria | rel=r_associated | relid=0 | w=30
  271. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:d-glyceric aciduria
    n1=en:deafness, autosomal recessive 1a | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=30
  272. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:deafness, autosomal recessive 28
    n1=en:deafness, autosomal recessive 1a | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=30
  273. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:duane syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:duane syndrome | rel=r_associated | relid=0 | w=30
  274. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:empty sella syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=30
  275. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:familial dysautonomia
    n1=en:deafness, autosomal recessive 1a | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=30
  276. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:friedreich ataxia
    n1=en:deafness, autosomal recessive 1a | n2=en:friedreich ataxia | rel=r_associated | relid=0 | w=30
  277. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:frontotemporal dementia
    n1=en:deafness, autosomal recessive 1a | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
  278. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:gjb2, 1-bp del, 35g (dbsnp rs80338939)
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 1-bp del, 35g (dbsnp rs80338939) | rel=r_associated | relid=0 | w=30
  279. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:gjb2, glu47ter
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, glu47ter | rel=r_associated | relid=0 | w=30
  280. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:gjb2, val37ile
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, val37ile | rel=r_associated | relid=0 | w=30
  281. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:gyrate atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=30
  282. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:hereditary mucosal leukokeratosis
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=30
  283. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:hyperglycerolemia
    n1=en:deafness, autosomal recessive 1a | n2=en:hyperglycerolemia | rel=r_associated | relid=0 | w=30
  284. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=30
  285. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:ichthyosis
    n1=en:deafness, autosomal recessive 1a | n2=en:ichthyosis | rel=r_associated | relid=0 | w=30
  286. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:imperforate anus
    n1=en:deafness, autosomal recessive 1a | n2=en:imperforate anus | rel=r_associated | relid=0 | w=30
  287. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:incontinentia pigmenti
    n1=en:deafness, autosomal recessive 1a | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=30
  288. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:juvenile x-linked retinoschisis
    n1=en:deafness, autosomal recessive 1a | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=30
  289. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:klippel-trenaunay-weber syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=30
  290. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:lecithin acyltransferase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=30
  291. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:lennox-gastaut syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=30
  292. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:mansonelliasis
    n1=en:deafness, autosomal recessive 1a | n2=en:mansonelliasis | rel=r_associated | relid=0 | w=30
  293. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:mowat-wilson syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=30
  294. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:myositis
    n1=en:deafness, autosomal recessive 1a | n2=en:myositis | rel=r_associated | relid=0 | w=30
  295. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:neural tube defect
    n1=en:deafness, autosomal recessive 1a | n2=en:neural tube defect | rel=r_associated | relid=0 | w=30
  296. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:noise induced deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:noise induced deafness | rel=r_associated | relid=0 | w=30
  297. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:orofaciodigital syndrome type 6
    n1=en:deafness, autosomal recessive 1a | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=30
  298. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:pemphigoid gestationis
    n1=en:deafness, autosomal recessive 1a | n2=en:pemphigoid gestationis | rel=r_associated | relid=0 | w=30
  299. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:piebaldism
    n1=en:deafness, autosomal recessive 1a | n2=en:piebaldism | rel=r_associated | relid=0 | w=30
  300. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:russell-silver syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=30
  301. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:sea-blue histiocyte syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=30
  302. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:selective antibody deficiency with normal immunoglobulins
    n1=en:deafness, autosomal recessive 1a | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=30
  303. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:septo-optic dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=30
  304. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:sitosterolemia
    n1=en:deafness, autosomal recessive 1a | n2=en:sitosterolemia | rel=r_associated | relid=0 | w=30
  305. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:smith-lemli-opitz syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=30
  306. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:spasmodic torticollis
    n1=en:deafness, autosomal recessive 1a | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=30
  307. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:spondyloepimetaphyseal dysplasia, sponastrime type
    n1=en:deafness, autosomal recessive 1a | n2=en:spondyloepimetaphyseal dysplasia, sponastrime type | rel=r_associated | relid=0 | w=30
  308. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:sudden unexplained death in childhood
    n1=en:deafness, autosomal recessive 1a | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=30
  309. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:superior mesenteric artery syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=30
  310. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:surfactant protein deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=30
  311. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:thanatophoric dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=30
  312. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:trichorhinophalangeal syndrome type i
    n1=en:deafness, autosomal recessive 1a | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=30
  313. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:turner syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:turner syndrome | rel=r_associated | relid=0 | w=30
  314. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:uniparental disomy
    n1=en:deafness, autosomal recessive 1a | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=30
  315. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:uveomeningoencephalitic syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=30
  316. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:vestibular dysfunction (in some patients)
    n1=en:deafness, autosomal recessive 1a | n2=en:vestibular dysfunction (in some patients) | rel=r_associated | relid=0 | w=30
  317. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:wallerian degeneration
    n1=en:deafness, autosomal recessive 1a | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=30
  318. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:x-linked bulbar-muscular atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=30
  319. en:deafness, autosomal recessive 1a -- r_associated #0: 30 / 0.698 -> en:xyy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=30
  320. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:1p36 deletion syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=29
  321. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:22q telomere deletion syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=29
  322. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:achondrogenesis
    n1=en:deafness, autosomal recessive 1a | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=29
  323. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=29
  324. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:aicardi syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=29
  325. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:anencephaly
    n1=en:deafness, autosomal recessive 1a | n2=en:anencephaly | rel=r_associated | relid=0 | w=29
  326. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:autoimmune polyendocrinopathy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=29
  327. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:carnitine palmitoyltransferase i deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=29
  328. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:cryopyrin-associated periodic syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=29
  329. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:cystinuria
    n1=en:deafness, autosomal recessive 1a | n2=en:cystinuria | rel=r_associated | relid=0 | w=29
  330. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:deletion 18p syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=29
  331. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:digenic dominant
    n1=en:deafness, autosomal recessive 1a | n2=en:digenic dominant | rel=r_associated | relid=0 | w=29
  332. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:donohue syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=29
  333. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:encephalocele
    n1=en:deafness, autosomal recessive 1a | n2=en:encephalocele | rel=r_associated | relid=0 | w=29
  334. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:fibromuscular dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:fibromuscular dysplasia | rel=r_associated | relid=0 | w=29
  335. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:frontonasal dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=29
  336. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:gangrenous stomatitis
    n1=en:deafness, autosomal recessive 1a | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=29
  337. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:gerstmann-straussler-scheinker disease
    n1=en:deafness, autosomal recessive 1a | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=29
  338. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:gjb2, 14-bp del, nt313
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 14-bp del, nt313 | rel=r_associated | relid=0 | w=29
  339. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:gjb2, arg184pro
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, arg184pro | rel=r_associated | relid=0 | w=29
  340. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:griscelli syndrome type 2
    n1=en:deafness, autosomal recessive 1a | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=29
  341. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hartnup disease
    n1=en:deafness, autosomal recessive 1a | n2=en:hartnup disease | rel=r_associated | relid=0 | w=29
  342. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hearing loss, profound prelingual sensorineural
    n1=en:deafness, autosomal recessive 1a | n2=en:hearing loss, profound prelingual sensorineural | rel=r_associated | relid=0 | w=29
  343. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hereditary angioedema
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=29
  344. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hereditary fructose intolerance
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=29
  345. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:high molecular weight kininogen deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=29
  346. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:holocarboxylase synthetase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=29
  347. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:homocystinuria
    n1=en:deafness, autosomal recessive 1a | n2=en:homocystinuria | rel=r_associated | relid=0 | w=29
  348. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hyaline membrane syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=29
  349. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hymenolepiasis
    n1=en:deafness, autosomal recessive 1a | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=29
  350. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:hypoalphalipoproteinemia
    n1=en:deafness, autosomal recessive 1a | n2=en:hypoalphalipoproteinemia | rel=r_associated | relid=0 | w=29
  351. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:immunodeficiency with hyper-igm type 2
    n1=en:deafness, autosomal recessive 1a | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=29
  352. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:intestinal atresia
    n1=en:deafness, autosomal recessive 1a | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=29
  353. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:kartagener syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=29
  354. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:kernicterus
    n1=en:deafness, autosomal recessive 1a | n2=en:kernicterus | rel=r_associated | relid=0 | w=29
  355. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:lafora disease
    n1=en:deafness, autosomal recessive 1a | n2=en:lafora disease | rel=r_associated | relid=0 | w=29
  356. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:lig4 syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=29
  357. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:lysinuric protein intolerance
    n1=en:deafness, autosomal recessive 1a | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=29
  358. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:malakoplakia
    n1=en:deafness, autosomal recessive 1a | n2=en:malakoplakia | rel=r_associated | relid=0 | w=29
  359. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:melorheostosis
    n1=en:deafness, autosomal recessive 1a | n2=en:melorheostosis | rel=r_associated | relid=0 | w=29
  360. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:methionine adenosyltransferase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=29
  361. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=29
  362. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:migrating partial seizures in infancy
    n1=en:deafness, autosomal recessive 1a | n2=en:migrating partial seizures in infancy | rel=r_associated | relid=0 | w=29
  363. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:moyamoya disease
    n1=en:deafness, autosomal recessive 1a | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=29
  364. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:neurotoxicity syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=29
  365. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:pallister-hall syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=29
  366. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:pelizaeus-merzbacher disease
    n1=en:deafness, autosomal recessive 1a | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=29
  367. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:persistent fetal circulation
    n1=en:deafness, autosomal recessive 1a | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=29
  368. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:primary hypertrophic osteoarthropathy
    n1=en:deafness, autosomal recessive 1a | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=29
  369. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:prune belly syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=29
  370. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:pseudoachondroplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=29
  371. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:pseudohermaphroditism
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudohermaphroditism | rel=r_associated | relid=0 | w=29
  372. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:pseudotumor cerebri
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=29
  373. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:scleromyxedema
    n1=en:deafness, autosomal recessive 1a | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=29
  374. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:spondyloepimetaphyseal dysplasia with joint laxity type 2
    n1=en:deafness, autosomal recessive 1a | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=29
  375. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:stickler syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=29
  376. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:takotsubo cardiomyopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=29
  377. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:tangier disease
    n1=en:deafness, autosomal recessive 1a | n2=en:tangier disease | rel=r_associated | relid=0 | w=29
  378. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:thyroid dysgenesis
    n1=en:deafness, autosomal recessive 1a | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=29
  379. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:toxic deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:toxic deafness | rel=r_associated | relid=0 | w=29
  380. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> en:wegener granulomatosis
    n1=en:deafness, autosomal recessive 1a | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=29
  381. en:deafness, autosomal recessive 1a -- r_associated #0: 29 / 0.674 -> paralysies périodiques familiales
    n1=en:deafness, autosomal recessive 1a | n2=paralysies périodiques familiales | rel=r_associated | relid=0 | w=29
  382. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:acrocephalosyndactyly
    n1=en:deafness, autosomal recessive 1a | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=28
  383. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=28
  384. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:andersen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=28
  385. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:antithrombin iii deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=28
  386. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:bartter syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=28
  387. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:brain iron accumulation type i syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=28
  388. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:congenital cortical hyperostosis
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=28
  389. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:congenital myasthenic syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=28
  390. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:dandy-walker malformation
    n1=en:deafness, autosomal recessive 1a | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=28
  391. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:de sanctis-cacchione syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=28
  392. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:deafness, autosomal recessive 49
    n1=en:deafness, autosomal recessive 1a | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=28
  393. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:dubowitz syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=28
  394. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:ectodermal dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=28
  395. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:episodic pain syndrome, familial, 3
    n1=en:deafness, autosomal recessive 1a | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=28
  396. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:erythrokeratodermia variabilis
    n1=en:deafness, autosomal recessive 1a | n2=en:erythrokeratodermia variabilis | rel=r_associated | relid=0 | w=28
  397. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:erythropoietic porphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=28
  398. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:erythropoietic protoporphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=28
  399. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:feingold syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=28
  400. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:fraser syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=28
  401. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:gjb2, 5-bp dup, nt280
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, 5-bp dup, nt280 | rel=r_associated | relid=0 | w=28
  402. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:gjb2, ivs1ds, g-a, +1
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, ivs1ds, g-a, +1 | rel=r_associated | relid=0 | w=28
  403. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:gjb2, trp77ter
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, trp77ter | rel=r_associated | relid=0 | w=28
  404. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:glutaric acidemia type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=28
  405. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:hajdu-cheney syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=28
  406. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:hard skin syndrome parana type
    n1=en:deafness, autosomal recessive 1a | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=28
  407. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:hearing impaired persons
    n1=en:deafness, autosomal recessive 1a | n2=en:hearing impaired persons | rel=r_associated | relid=0 | w=28
  408. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:holmes-adie syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=28
  409. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:imperforate vagina
    n1=en:deafness, autosomal recessive 1a | n2=en:imperforate vagina | rel=r_associated | relid=0 | w=28
  410. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:kluver-bucy syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=28
  411. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:kniest dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:kniest dysplasia | rel=r_associated | relid=0 | w=28
  412. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:landau-kleffner syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=28
  413. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:lesch-nyhan syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=28
  414. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:leukodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=28
  415. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=28
  416. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:marshall syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=28
  417. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:muscular dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=28
  418. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:myokymia
    n1=en:deafness, autosomal recessive 1a | n2=en:myokymia | rel=r_associated | relid=0 | w=28
  419. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:other specified hearing loss
    n1=en:deafness, autosomal recessive 1a | n2=en:other specified hearing loss | rel=r_associated | relid=0 | w=28
  420. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:otopalatodigital syndrome type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=28
  421. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:pantothenate kinase-associated neurodegeneration
    n1=en:deafness, autosomal recessive 1a | n2=en:pantothenate kinase-associated neurodegeneration | rel=r_associated | relid=0 | w=28
  422. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:paroxysmal extreme pain disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=28
  423. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:peritoneal panniculitis
    n1=en:deafness, autosomal recessive 1a | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=28
  424. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:potocki-shaffer syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=28
  425. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:progressive bulbar palsy
    n1=en:deafness, autosomal recessive 1a | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=28
  426. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:progressive supranuclear palsy
    n1=en:deafness, autosomal recessive 1a | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=28
  427. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:short rib-polydactyly syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=28
  428. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:short stature homeobox deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=28
  429. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:shy-drager syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=28
  430. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:status epilepticus
    n1=en:deafness, autosomal recessive 1a | n2=en:status epilepticus | rel=r_associated | relid=0 | w=28
  431. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:sweet syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=28
  432. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:trichorhinophalangeal syndrome type ii
    n1=en:deafness, autosomal recessive 1a | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=28
  433. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:trigger finger disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=28
  434. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> en:waardenburg syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=28
  435. en:deafness, autosomal recessive 1a -- r_associated #0: 28 / 0.651 -> peste
    (maladie)
    n1=en:deafness, autosomal recessive 1a | n2=peste
    (maladie)
    | rel=r_associated | relid=0 | w=28
  436. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:achenbach syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=27
  437. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:ainhum
    n1=en:deafness, autosomal recessive 1a | n2=en:ainhum | rel=r_associated | relid=0 | w=27
  438. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:allan-herndon-dudley syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=27
  439. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:alstrom syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=27
  440. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:analbuminemia
    n1=en:deafness, autosomal recessive 1a | n2=en:analbuminemia | rel=r_associated | relid=0 | w=27
  441. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=27
  442. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:atrophic muscular disorder
    n1=en:deafness, autosomal recessive 1a | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=27
  443. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:autosomal recessive inheritance
    n1=en:deafness, autosomal recessive 1a | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=27
  444. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:carbohydrate-deficient glycoprotein syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=27
  445. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:cataplexy
    n1=en:deafness, autosomal recessive 1a | n2=en:cataplexy | rel=r_associated | relid=0 | w=27
  446. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:chilblains
    n1=en:deafness, autosomal recessive 1a | n2=en:chilblains | rel=r_associated | relid=0 | w=27
  447. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:chondrodysplasia punctata
    n1=en:deafness, autosomal recessive 1a | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=27
  448. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:combined lipase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=27
  449. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:complex regional pain syndrome i
    n1=en:deafness, autosomal recessive 1a | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=27
  450. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:congenital deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:congenital deafness | rel=r_associated | relid=0 | w=27
  451. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:cor triatriatum
    n1=en:deafness, autosomal recessive 1a | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=27
  452. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:cranioectodermal dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=27
  453. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:d-bifunctional protein deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:d-bifunctional protein deficiency | rel=r_associated | relid=0 | w=27
  454. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:darier disease
    n1=en:deafness, autosomal recessive 1a | n2=en:darier disease | rel=r_associated | relid=0 | w=27
  455. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:deafness, digenic, gjb2/gjb6 (disorder)
    n1=en:deafness, autosomal recessive 1a | n2=en:deafness, digenic, gjb2/gjb6 (disorder) | rel=r_associated | relid=0 | w=27
  456. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=27
  457. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:diffuse idiopathic skeletal hyperostosis
    n1=en:deafness, autosomal recessive 1a | n2=en:diffuse idiopathic skeletal hyperostosis | rel=r_associated | relid=0 | w=27
  458. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:familial hypertrophic cardiomyopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=27
  459. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:fibrodysplasia ossificans progressiva
    n1=en:deafness, autosomal recessive 1a | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=27
  460. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:gastric antral vascular ectasia
    n1=en:deafness, autosomal recessive 1a | n2=en:gastric antral vascular ectasia | rel=r_associated | relid=0 | w=27
  461. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:generalized arterial calcification of infancy 1
    n1=en:deafness, autosomal recessive 1a | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=27
  462. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:genu varum
    n1=en:deafness, autosomal recessive 1a | n2=en:genu varum | rel=r_associated | relid=0 | w=27
  463. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:gitelman syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=27
  464. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:gjb2, asp159val
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, asp159val | rel=r_associated | relid=0 | w=27
  465. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  466. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:goldenhar syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=27
  467. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:hemorrhagic fever with renal syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hemorrhagic fever with renal syndrome | rel=r_associated | relid=0 | w=27
  468. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:hereditary coproporphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=27
  469. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:heritable pulmonary arterial hypertension
    n1=en:deafness, autosomal recessive 1a | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=27
  470. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:hypophosphatasia
    n1=en:deafness, autosomal recessive 1a | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=27
  471. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:idiopathic hypersomnolence
    n1=en:deafness, autosomal recessive 1a | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=27
  472. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:immunoglobulin a deficiency 1
    n1=en:deafness, autosomal recessive 1a | n2=en:immunoglobulin a deficiency 1 | rel=r_associated | relid=0 | w=27
  473. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:iridocorneal endothelial syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=27
  474. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:klippel-feil syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=27
  475. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:mitochondrial trifunctional protein deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=27
  476. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:mobius syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=27
  477. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:nelson syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=27
  478. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:nephrocalcinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=27
  479. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:neuronal intranuclear inclusion disease
    n1=en:deafness, autosomal recessive 1a | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=27
  480. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:neuropathy, hereditary sensory and autonomic, type vii
    n1=en:deafness, autosomal recessive 1a | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=27
  481. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:norrie syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=27
  482. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:pachyonychia congenita
    n1=en:deafness, autosomal recessive 1a | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=27
  483. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:pentalogy of cantrell
    n1=en:deafness, autosomal recessive 1a | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=27
  484. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:peters-plus syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=27
  485. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:phosphoenolpyruvate carboxykinase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=27
  486. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:piriformis muscle syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=27
  487. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:pityriasis lichenoides
    n1=en:deafness, autosomal recessive 1a | n2=en:pityriasis lichenoides | rel=r_associated | relid=0 | w=27
  488. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:poland syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:poland syndrome | rel=r_associated | relid=0 | w=27
  489. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:porokeratosis
    n1=en:deafness, autosomal recessive 1a | n2=en:porokeratosis | rel=r_associated | relid=0 | w=27
  490. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:pyruvate dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  491. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:rieger syndrome type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=27
  492. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:sjogren-larsson syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=27
  493. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:sotos syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=27
  494. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:spinal muscular atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=27
  495. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:togaviridae infection
    n1=en:deafness, autosomal recessive 1a | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=27
  496. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:tooth and nail syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=27
  497. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:tracheobronchomegaly
    n1=en:deafness, autosomal recessive 1a | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=27
  498. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:weill-marchesani syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=27
  499. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:williams syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:williams syndrome | rel=r_associated | relid=0 | w=27
  500. en:deafness, autosomal recessive 1a -- r_associated #0: 27 / 0.628 -> en:yellow nail syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=27
  501. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:amaurosis fugax
    n1=en:deafness, autosomal recessive 1a | n2=en:amaurosis fugax | rel=r_associated | relid=0 | w=26
  502. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:bernard-soulier syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=26
  503. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:calciphylaxis
    n1=en:deafness, autosomal recessive 1a | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=26
  504. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:camurati-engelmann syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=26
  505. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:cardiofaciocutaneous syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=26
  506. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:caroli disease
    n1=en:deafness, autosomal recessive 1a | n2=en:caroli disease | rel=r_associated | relid=0 | w=26
  507. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:cerebrooculofacioskeletal syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=26
  508. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:connexin 26 gene anomaly
    n1=en:deafness, autosomal recessive 1a | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=26
  509. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:deafness, digenic, gjb2/gjb3 (disorder)
    n1=en:deafness, autosomal recessive 1a | n2=en:deafness, digenic, gjb2/gjb3 (disorder) | rel=r_associated | relid=0 | w=26
  510. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:deletion 18q syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=26
  511. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:dentinogenesis imperfecta
    n1=en:deafness, autosomal recessive 1a | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=26
  512. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:drug- and toxin-induced pulmonary arterial hypertension
    n1=en:deafness, autosomal recessive 1a | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=26
  513. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:ear
    n1=en:deafness, autosomal recessive 1a | n2=en:ear | rel=r_associated | relid=0 | w=26
  514. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:ectrodactyly
    n1=en:deafness, autosomal recessive 1a | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=26
  515. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:exfoliation syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=26
  516. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:farber lipogranulomatosis
    n1=en:deafness, autosomal recessive 1a | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=26
  517. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:gjb2, -3438c-t
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, -3438c-t | rel=r_associated | relid=0 | w=26
  518. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:gjb2, arg143trp
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, arg143trp | rel=r_associated | relid=0 | w=26
  519. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:gjb2, gly45glu
    n1=en:deafness, autosomal recessive 1a | n2=en:gjb2, gly45glu | rel=r_associated | relid=0 | w=26
  520. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:glanzmann thrombasthenia
    n1=en:deafness, autosomal recessive 1a | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=26
  521. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hantavirus pulmonary syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=26
  522. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hepatolenticular degeneration
    n1=en:deafness, autosomal recessive 1a | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=26
  523. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hereditary persistence of fetal hemoglobin
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=26
  524. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:high frequency hearing loss
    n1=en:deafness, autosomal recessive 1a | n2=en:high frequency hearing loss | rel=r_associated | relid=0 | w=26
  525. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hmg-coa lyase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=26
  526. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:holt-oram syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=26
  527. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hydroa vacciniforme
    n1=en:deafness, autosomal recessive 1a | n2=en:hydroa vacciniforme | rel=r_associated | relid=0 | w=26
  528. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:hypokalemic periodic paralysis
    n1=en:deafness, autosomal recessive 1a | n2=en:hypokalemic periodic paralysis | rel=r_associated | relid=0 | w=26
  529. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:jeune syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=26
  530. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:joubert syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=26
  531. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:kallmann syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=26
  532. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:leber congenital amaurosis
    n1=en:deafness, autosomal recessive 1a | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=26
  533. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:levocardia
    n1=en:deafness, autosomal recessive 1a | n2=en:levocardia | rel=r_associated | relid=0 | w=26
  534. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
  535. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:mallory-weiss syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=26
  536. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:meesmann corneal dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=26
  537. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:methylmalonic acidemia
    n1=en:deafness, autosomal recessive 1a | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=26
  538. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:molybdenum cofactor deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=26
  539. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:monilethrix
    n1=en:deafness, autosomal recessive 1a | n2=en:monilethrix | rel=r_associated | relid=0 | w=26
  540. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:multiple system atrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=26
  541. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:nephrogenic fibrosing dermopathy
    n1=en:deafness, autosomal recessive 1a | n2=en:nephrogenic fibrosing dermopathy | rel=r_associated | relid=0 | w=26
  542. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:oculocerebrorenal syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=26
  543. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:osteopetrosis with renal tubular acidosis
    n1=en:deafness, autosomal recessive 1a | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=26
  544. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:other specified forms of deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:other specified forms of deafness | rel=r_associated | relid=0 | w=26
  545. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:pallister-killian syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=26
  546. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:pancreatic lipase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:pancreatic lipase deficiency | rel=r_associated | relid=0 | w=26
  547. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:progeria
    n1=en:deafness, autosomal recessive 1a | n2=en:progeria | rel=r_associated | relid=0 | w=26
  548. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:prolidase deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=26
  549. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:prosopagnosia
    n1=en:deafness, autosomal recessive 1a | n2=en:prosopagnosia | rel=r_associated | relid=0 | w=26
  550. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:pseudotrisomy 13 syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  551. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=26
  552. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:sudden unexplained infant death
    n1=en:deafness, autosomal recessive 1a | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=26
  553. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:thoracic outlet syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=26
  554. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:tolosa-hunt syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=26
  555. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:transposition of great vessels
    n1=en:deafness, autosomal recessive 1a | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=26
  556. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:trichinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:trichinosis | rel=r_associated | relid=0 | w=26
  557. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:true hermaphroditism
    n1=en:deafness, autosomal recessive 1a | n2=en:true hermaphroditism | rel=r_associated | relid=0 | w=26
  558. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:vitelliform macular dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=26
  559. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:west syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:west syndrome | rel=r_associated | relid=0 | w=26
  560. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:whipple disease
    n1=en:deafness, autosomal recessive 1a | n2=en:whipple disease | rel=r_associated | relid=0 | w=26
  561. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:wolfram syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=26
  562. en:deafness, autosomal recessive 1a -- r_associated #0: 26 / 0.605 -> en:x-linked creatine transporter deficiency
    n1=en:deafness, autosomal recessive 1a | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=26
  563. en:deafness, autosomal recessive 1a -- r_associated #0: 25 / 0.581 -> perte d'audition sensorineurale
    n1=en:deafness, autosomal recessive 1a | n2=perte d'audition sensorineurale | rel=r_associated | relid=0 | w=25
  564. en:deafness, autosomal recessive 1a -- r_associated #0: 23 / 0.535 -> maladie de Marfan
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Marfan | rel=r_associated | relid=0 | w=23
  565. en:deafness, autosomal recessive 1a -- r_associated #0: 23 / 0.535 -> syndrome de Marfan
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=23
  566. en:deafness, autosomal recessive 1a -- r_associated #0: 22 / 0.512 -> surdité congénitale
    n1=en:deafness, autosomal recessive 1a | n2=surdité congénitale | rel=r_associated | relid=0 | w=22
  567. en:deafness, autosomal recessive 1a -- r_associated #0: 21 / 0.488 -> surdité héréditaire
    n1=en:deafness, autosomal recessive 1a | n2=surdité héréditaire | rel=r_associated | relid=0 | w=21
  568. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acidémie glutarique de type 1
    n1=en:deafness, autosomal recessive 1a | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  569. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acidurie glutarique de type 1
    n1=en:deafness, autosomal recessive 1a | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  570. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:deafness, autosomal recessive 1a | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  571. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acromégalie
    n1=en:deafness, autosomal recessive 1a | n2=acromégalie | rel=r_associated | relid=0 | w=20
  572. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens
    n1=en:deafness, autosomal recessive 1a | n2=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | rel=r_associated | relid=0 | w=20
  573. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> acromegaly
    n1=en:deafness, autosomal recessive 1a | n2=acromegaly | rel=r_associated | relid=0 | w=20
  574. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> agnosie
    n1=en:deafness, autosomal recessive 1a | n2=agnosie | rel=r_associated | relid=0 | w=20
  575. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aïnhum
    n1=en:deafness, autosomal recessive 1a | n2=aïnhum | rel=r_associated | relid=0 | w=20
  576. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ainhum
    n1=en:deafness, autosomal recessive 1a | n2=ainhum | rel=r_associated | relid=0 | w=20
  577. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> albinisme
    n1=en:deafness, autosomal recessive 1a | n2=albinisme | rel=r_associated | relid=0 | w=20
  578. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> albinisme oculocutané de type mutant jaune
    n1=en:deafness, autosomal recessive 1a | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  579. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> analbuminémie
    n1=en:deafness, autosomal recessive 1a | n2=analbuminémie | rel=r_associated | relid=0 | w=20
  580. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> anasarque foetal
    n1=en:deafness, autosomal recessive 1a | n2=anasarque foetal | rel=r_associated | relid=0 | w=20
  581. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> anasarque foeto-placentaire
    n1=en:deafness, autosomal recessive 1a | n2=anasarque foeto-placentaire | rel=r_associated | relid=0 | w=20
  582. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> anasarque foetoplacentaire
    n1=en:deafness, autosomal recessive 1a | n2=anasarque foetoplacentaire | rel=r_associated | relid=0 | w=20
  583. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> anencéphalie
    n1=en:deafness, autosomal recessive 1a | n2=anencéphalie | rel=r_associated | relid=0 | w=20
  584. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aniridie, microcornée et cataracte régressive
    n1=en:deafness, autosomal recessive 1a | n2=aniridie, microcornée et cataracte régressive | rel=r_associated | relid=0 | w=20
  585. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> anomalie d'Ebstein
    n1=en:deafness, autosomal recessive 1a | n2=anomalie d'Ebstein | rel=r_associated | relid=0 | w=20
  586. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aphasie primaire progressive
    n1=en:deafness, autosomal recessive 1a | n2=aphasie primaire progressive | rel=r_associated | relid=0 | w=20
  587. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aphasie progressive primaire
    n1=en:deafness, autosomal recessive 1a | n2=aphasie progressive primaire | rel=r_associated | relid=0 | w=20
  588. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aphasies primaires progressives
    n1=en:deafness, autosomal recessive 1a | n2=aphasies primaires progressives | rel=r_associated | relid=0 | w=20
  589. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> aplasie de la paroi abdominale
    n1=en:deafness, autosomal recessive 1a | n2=aplasie de la paroi abdominale | rel=r_associated | relid=0 | w=20
  590. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> arachnodactylie
    n1=en:deafness, autosomal recessive 1a | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  591. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> arthrogrypose
    n1=en:deafness, autosomal recessive 1a | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
  592. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> atrophie optique autosomique dominante
    n1=en:deafness, autosomal recessive 1a | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
  593. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cataplexie
    n1=en:deafness, autosomal recessive 1a | n2=cataplexie | rel=r_associated | relid=0 | w=20
  594. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> chondrodysplasia punctata
    n1=en:deafness, autosomal recessive 1a | n2=chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
  595. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> chondrodysplasie léthale avec brièveté des côtes
    n1=en:deafness, autosomal recessive 1a | n2=chondrodysplasie léthale avec brièveté des côtes | rel=r_associated | relid=0 | w=20
  596. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> coarctation aortique
    n1=en:deafness, autosomal recessive 1a | n2=coarctation aortique | rel=r_associated | relid=0 | w=20
  597. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> crânio-sténose
    n1=en:deafness, autosomal recessive 1a | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  598. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> craniosténose
    n1=en:deafness, autosomal recessive 1a | n2=craniosténose | rel=r_associated | relid=0 | w=20
  599. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> crâniosténose
    n1=en:deafness, autosomal recessive 1a | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  600. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> craniosynostose
    n1=en:deafness, autosomal recessive 1a | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  601. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> crâniosynostose
    n1=en:deafness, autosomal recessive 1a | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  602. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cysticercose
    n1=en:deafness, autosomal recessive 1a | n2=cysticercose | rel=r_associated | relid=0 | w=20
  603. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cysticercose cérébrale
    n1=en:deafness, autosomal recessive 1a | n2=cysticercose cérébrale | rel=r_associated | relid=0 | w=20
  604. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cysticercose du système nerveux central
    n1=en:deafness, autosomal recessive 1a | n2=cysticercose du système nerveux central | rel=r_associated | relid=0 | w=20
  605. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cysticercose neurologique
    n1=en:deafness, autosomal recessive 1a | n2=cysticercose neurologique | rel=r_associated | relid=0 | w=20
  606. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> cysticercoses
    n1=en:deafness, autosomal recessive 1a | n2=cysticercoses | rel=r_associated | relid=0 | w=20
  607. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficience auditive totale
    n1=en:deafness, autosomal recessive 1a | n2=déficience auditive totale | rel=r_associated | relid=0 | w=20
  608. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en biotinidase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20
  609. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  610. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  611. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  612. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  613. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en protéine trifonctionnelle mitochondriale
    n1=en:deafness, autosomal recessive 1a | n2=déficit en protéine trifonctionnelle mitochondriale | rel=r_associated | relid=0 | w=20
  614. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:deafness, autosomal recessive 1a | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  615. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> démence fronto-temporale
    n1=en:deafness, autosomal recessive 1a | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  616. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> démence frontotemporale
    n1=en:deafness, autosomal recessive 1a | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  617. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dentine opalescente héréditaire
    n1=en:deafness, autosomal recessive 1a | n2=dentine opalescente héréditaire | rel=r_associated | relid=0 | w=20
  618. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dentinogénèse imparfaite
    n1=en:deafness, autosomal recessive 1a | n2=dentinogénèse imparfaite | rel=r_associated | relid=0 | w=20
  619. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> DentinoGenesis Imperfecta
    n1=en:deafness, autosomal recessive 1a | n2=DentinoGenesis Imperfecta | rel=r_associated | relid=0 | w=20
  620. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dentinogenesis imperfecta
    n1=en:deafness, autosomal recessive 1a | n2=dentinogenesis imperfecta | rel=r_associated | relid=0 | w=20
  621. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dextrocardie
    n1=en:deafness, autosomal recessive 1a | n2=dextrocardie | rel=r_associated | relid=0 | w=20
  622. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> distomatoses pulmonaires
    n1=en:deafness, autosomal recessive 1a | n2=distomatoses pulmonaires | rel=r_associated | relid=0 | w=20
  623. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Duane (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Duane (syndrome de) | rel=r_associated | relid=0 | w=20
  624. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysérythropoïèse congénitale
    n1=en:deafness, autosomal recessive 1a | n2=dysérythropoïèse congénitale | rel=r_associated | relid=0 | w=20
  625. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysostose craniofaciale
    n1=en:deafness, autosomal recessive 1a | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20
  626. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie campomélique
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie campomélique | rel=r_associated | relid=0 | w=20
  627. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie cléido-crânienne
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
  628. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie cléidocrânienne
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
  629. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  630. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  631. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  632. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dysplasie frontonasale
    n1=en:deafness, autosomal recessive 1a | n2=dysplasie frontonasale | rel=r_associated | relid=0 | w=20
  633. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophie neuro-axonale infantile
    n1=en:deafness, autosomal recessive 1a | n2=dystrophie neuro-axonale infantile | rel=r_associated | relid=0 | w=20
  634. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale
    n1=en:deafness, autosomal recessive 1a | n2=dystrophie neuroaxonale | rel=r_associated | relid=0 | w=20
  635. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale de Seitelberger
    n1=en:deafness, autosomal recessive 1a | n2=dystrophie neuroaxonale de Seitelberger | rel=r_associated | relid=0 | w=20
  636. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale infantile
    n1=en:deafness, autosomal recessive 1a | n2=dystrophie neuroaxonale infantile | rel=r_associated | relid=0 | w=20
  637. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophie orbitaire congénitale
    n1=en:deafness, autosomal recessive 1a | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20
  638. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> dystrophies neuroaxonales
    n1=en:deafness, autosomal recessive 1a | n2=dystrophies neuroaxonales | rel=r_associated | relid=0 | w=20
  639. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:deafness, autosomal recessive 1a | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  640. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ectrodactylie
    n1=en:deafness, autosomal recessive 1a | n2=ectrodactylie | rel=r_associated | relid=0 | w=20
  641. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:alveolar proteinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:alveolar proteinosis | rel=r_associated | relid=0 | w=20
  642. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:anacusia
    n1=en:deafness, autosomal recessive 1a | n2=en:anacusia | rel=r_associated | relid=0 | w=20
  643. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:anacusis
    n1=en:deafness, autosomal recessive 1a | n2=en:anacusis | rel=r_associated | relid=0 | w=20
  644. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:anal imperforation
    n1=en:deafness, autosomal recessive 1a | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  645. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:and mental retardation
    n1=en:deafness, autosomal recessive 1a | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  646. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:anterior plagiocephalies, synostotic
    n1=en:deafness, autosomal recessive 1a | n2=en:anterior plagiocephalies, synostotic | rel=r_associated | relid=0 | w=20
  647. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:arachnodactily
    n1=en:deafness, autosomal recessive 1a | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
  648. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:arachnodactyly
    n1=en:deafness, autosomal recessive 1a | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  649. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:arnold chiari malformation
    n1=en:deafness, autosomal recessive 1a | n2=en:arnold chiari malformation | rel=r_associated | relid=0 | w=20
  650. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:arnold-chiari deformity
    n1=en:deafness, autosomal recessive 1a | n2=en:arnold-chiari deformity | rel=r_associated | relid=0 | w=20
  651. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:autosomal dominant congenital deafness with onychodystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
  652. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:black death
    n1=en:deafness, autosomal recessive 1a | n2=en:black death | rel=r_associated | relid=0 | w=20
  653. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Black death
    n1=en:deafness, autosomal recessive 1a | n2=en:Black death | rel=r_associated | relid=0 | w=20
  654. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:black plague
    n1=en:deafness, autosomal recessive 1a | n2=en:black plague | rel=r_associated | relid=0 | w=20
  655. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:deafness, autosomal recessive 1a | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  656. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cardio-facio-cutaneous syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:cardio-facio-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  657. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cataplexia
    n1=en:deafness, autosomal recessive 1a | n2=en:cataplexia | rel=r_associated | relid=0 | w=20
  658. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cataplexis
    n1=en:deafness, autosomal recessive 1a | n2=en:cataplexis | rel=r_associated | relid=0 | w=20
  659. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:CDA
    n1=en:deafness, autosomal recessive 1a | n2=en:CDA | rel=r_associated | relid=0 | w=20
  660. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cerebral gigantism
    n1=en:deafness, autosomal recessive 1a | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  661. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cerebral tuberculosis
    n1=en:deafness, autosomal recessive 1a | n2=en:cerebral tuberculosis | rel=r_associated | relid=0 | w=20
  662. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:deafness, autosomal recessive 1a | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  663. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cleft lip and palate
    n1=en:deafness, autosomal recessive 1a | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  664. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:coloboma and anal atresia syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:coloboma and anal atresia syndrome | rel=r_associated | relid=0 | w=20
  665. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:cysticercosis
    n1=en:deafness, autosomal recessive 1a | n2=en:cysticercosis | rel=r_associated | relid=0 | w=20
  666. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:dactylolysis spontanea
    n1=en:deafness, autosomal recessive 1a | n2=en:dactylolysis spontanea | rel=r_associated | relid=0 | w=20
  667. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Dercum's disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Dercum's disease | rel=r_associated | relid=0 | w=20
  668. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Devergie's disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Devergie's disease | rel=r_associated | relid=0 | w=20
  669. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Donohue syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Donohue syndrome | rel=r_associated | relid=0 | w=20
  670. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Duane's syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Duane's syndrome | rel=r_associated | relid=0 | w=20
  671. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:ENT doctor
    n1=en:deafness, autosomal recessive 1a | n2=en:ENT doctor | rel=r_associated | relid=0 | w=20
  672. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:ENT specialist
    n1=en:deafness, autosomal recessive 1a | n2=en:ENT specialist | rel=r_associated | relid=0 | w=20
  673. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:erythermalgia
    n1=en:deafness, autosomal recessive 1a | n2=en:erythermalgia | rel=r_associated | relid=0 | w=20
  674. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:erythropoietic uroporphyria
    n1=en:deafness, autosomal recessive 1a | n2=en:erythropoietic uroporphyria | rel=r_associated | relid=0 | w=20
  675. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Feingold syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Feingold syndrome | rel=r_associated | relid=0 | w=20
  676. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Fox-Fordyce disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Fox-Fordyce disease | rel=r_associated | relid=0 | w=20
  677. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:FPLD
    n1=en:deafness, autosomal recessive 1a | n2=en:FPLD | rel=r_associated | relid=0 | w=20
  678. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  679. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:glaucoma capsulare
    n1=en:deafness, autosomal recessive 1a | n2=en:glaucoma capsulare | rel=r_associated | relid=0 | w=20
  680. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:glutaric aciduria type 1 | rel=r_associated | relid=0 | w=20
  681. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria, type 1
    n1=en:deafness, autosomal recessive 1a | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
  682. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Goltz syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
  683. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Gray platelet syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Gray platelet syndrome | rel=r_associated | relid=0 | w=20
  684. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:hansenarium
    n1=en:deafness, autosomal recessive 1a | n2=en:hansenarium | rel=r_associated | relid=0 | w=20
  685. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:head and neck
    n1=en:deafness, autosomal recessive 1a | n2=en:head and neck | rel=r_associated | relid=0 | w=20
  686. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Hebra's pityriasis
    n1=en:deafness, autosomal recessive 1a | n2=en:Hebra's pityriasis | rel=r_associated | relid=0 | w=20
  687. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:hereditary deafness
    n1=en:deafness, autosomal recessive 1a | n2=en:hereditary deafness | rel=r_associated | relid=0 | w=20
  688. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:heterotaxy
    n1=en:deafness, autosomal recessive 1a | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  689. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:hydrops foetalis
    n1=en:deafness, autosomal recessive 1a | n2=en:hydrops foetalis | rel=r_associated | relid=0 | w=20
  690. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:ichthyosis vera
    n1=en:deafness, autosomal recessive 1a | n2=en:ichthyosis vera | rel=r_associated | relid=0 | w=20
  691. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Korsakoff syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Korsakoff syndrome | rel=r_associated | relid=0 | w=20
  692. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:lazar-house
    n1=en:deafness, autosomal recessive 1a | n2=en:lazar-house | rel=r_associated | relid=0 | w=20
  693. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:leper colony
    n1=en:deafness, autosomal recessive 1a | n2=en:leper colony | rel=r_associated | relid=0 | w=20
  694. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:leprosarium
    n1=en:deafness, autosomal recessive 1a | n2=en:leprosarium | rel=r_associated | relid=0 | w=20
  695. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:leprosary
    n1=en:deafness, autosomal recessive 1a | n2=en:leprosary | rel=r_associated | relid=0 | w=20
  696. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:deafness, autosomal recessive 1a | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  697. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:deafness, autosomal recessive 1a | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  698. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Marfan's disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  699. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  700. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Martin-Bell's syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Martin-Bell's syndrome | rel=r_associated | relid=0 | w=20
  701. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:neurological cysticercosis
    n1=en:deafness, autosomal recessive 1a | n2=en:neurological cysticercosis | rel=r_associated | relid=0 | w=20
  702. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:nose and throat specialist
    n1=en:deafness, autosomal recessive 1a | n2=en:nose and throat specialist | rel=r_associated | relid=0 | w=20
  703. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:odontogenesis imperfecta
    n1=en:deafness, autosomal recessive 1a | n2=en:odontogenesis imperfecta | rel=r_associated | relid=0 | w=20
  704. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:ophthalmoneuritis
    n1=en:deafness, autosomal recessive 1a | n2=en:ophthalmoneuritis | rel=r_associated | relid=0 | w=20
  705. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:osteopoecilia
    n1=en:deafness, autosomal recessive 1a | n2=en:osteopoecilia | rel=r_associated | relid=0 | w=20
  706. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:otorhinolaryngologist
    n1=en:deafness, autosomal recessive 1a | n2=en:otorhinolaryngologist | rel=r_associated | relid=0 | w=20
  707. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Pick's disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Pick's disease | rel=r_associated | relid=0 | w=20
  708. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Plummer-Vinson syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Plummer-Vinson syndrome | rel=r_associated | relid=0 | w=20
  709. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:sarcitis
    n1=en:deafness, autosomal recessive 1a | n2=en:sarcitis | rel=r_associated | relid=0 | w=20
  710. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Seitelberger's neuroaxonal dystrophy
    n1=en:deafness, autosomal recessive 1a | n2=en:Seitelberger's neuroaxonal dystrophy | rel=r_associated | relid=0 | w=20
  711. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:situs inversus
    n1=en:deafness, autosomal recessive 1a | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  712. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:situs inversus viscerum
    n1=en:deafness, autosomal recessive 1a | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  713. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:situs mutatus
    n1=en:deafness, autosomal recessive 1a | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  714. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Soto's syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  715. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:sotos' syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  716. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Sotos' syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  717. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  718. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:deafness, autosomal recessive 1a | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  719. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:trichorhinophalangeal syndrome type II
    n1=en:deafness, autosomal recessive 1a | n2=en:trichorhinophalangeal syndrome type II | rel=r_associated | relid=0 | w=20
  720. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:tuberculosis of meninges (cerebral)(spinal)
    n1=en:deafness, autosomal recessive 1a | n2=en:tuberculosis of meninges (cerebral)(spinal) | rel=r_associated | relid=0 | w=20
  721. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:tuberculosis, meningeal
    n1=en:deafness, autosomal recessive 1a | n2=en:tuberculosis, meningeal | rel=r_associated | relid=0 | w=20
  722. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:tuberculous hypertrophic pachymeningitides
    n1=en:deafness, autosomal recessive 1a | n2=en:tuberculous hypertrophic pachymeningitides | rel=r_associated | relid=0 | w=20
  723. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:tuberculous leptomeningitis
    n1=en:deafness, autosomal recessive 1a | n2=en:tuberculous leptomeningitis | rel=r_associated | relid=0 | w=20
  724. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:tuberculous meningitis
    n1=en:deafness, autosomal recessive 1a | n2=en:tuberculous meningitis | rel=r_associated | relid=0 | w=20
  725. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Waterhouse-Friderichsen syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Waterhouse-Friderichsen syndrome | rel=r_associated | relid=0 | w=20
  726. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Whipple disease
    n1=en:deafness, autosomal recessive 1a | n2=en:Whipple disease | rel=r_associated | relid=0 | w=20
  727. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> en:Williams syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  728. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> érythermalgie
    n1=en:deafness, autosomal recessive 1a | n2=érythermalgie | rel=r_associated | relid=0 | w=20
  729. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> erythromelalgia
    n1=en:deafness, autosomal recessive 1a | n2=erythromelalgia | rel=r_associated | relid=0 | w=20
  730. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> érythromélalgie
    n1=en:deafness, autosomal recessive 1a | n2=érythromélalgie | rel=r_associated | relid=0 | w=20
  731. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> esgourde
    n1=en:deafness, autosomal recessive 1a | n2=esgourde | rel=r_associated | relid=0 | w=20
  732. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> examen non précisé, méningite tuberculeuse
    n1=en:deafness, autosomal recessive 1a | n2=examen non précisé, méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  733. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> gigantisme cérébral
    n1=en:deafness, autosomal recessive 1a | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  734. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> glaucome capsulaire
    n1=en:deafness, autosomal recessive 1a | n2=glaucome capsulaire | rel=r_associated | relid=0 | w=20
  735. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Goltz
    n1=en:deafness, autosomal recessive 1a | n2=Goltz | rel=r_associated | relid=0 | w=20
  736. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Goltz (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  737. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:deafness, autosomal recessive 1a | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  738. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:deafness, autosomal recessive 1a | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  739. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hétérotaxie
    n1=en:deafness, autosomal recessive 1a | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  740. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> holoprosencéphalie
    n1=en:deafness, autosomal recessive 1a | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
  741. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 2
    n1=en:deafness, autosomal recessive 1a | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
  742. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 3
    n1=en:deafness, autosomal recessive 1a | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
  743. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 4
    n1=en:deafness, autosomal recessive 1a | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
  744. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> holoprosencéphalie familiale alobaire de type 1
    n1=en:deafness, autosomal recessive 1a | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
  745. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hydroa vacciniforme
    n1=en:deafness, autosomal recessive 1a | n2=hydroa vacciniforme | rel=r_associated | relid=0 | w=20
  746. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hydroa vacciniforme de Bazin
    n1=en:deafness, autosomal recessive 1a | n2=hydroa vacciniforme de Bazin | rel=r_associated | relid=0 | w=20
  747. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hydrops foetoplacentaire
    n1=en:deafness, autosomal recessive 1a | n2=hydrops foetoplacentaire | rel=r_associated | relid=0 | w=20
  748. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hypoplasie dermique en aires
    n1=en:deafness, autosomal recessive 1a | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
  749. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> hypoplasie dermique focale
    n1=en:deafness, autosomal recessive 1a | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
  750. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ichthyose
    n1=en:deafness, autosomal recessive 1a | n2=ichthyose | rel=r_associated | relid=0 | w=20
  751. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ichtyose
    n1=en:deafness, autosomal recessive 1a | n2=ichtyose | rel=r_associated | relid=0 | w=20
  752. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ichtyose folliculaire, atrichie et photophobie
    n1=en:deafness, autosomal recessive 1a | n2=ichtyose folliculaire, atrichie et photophobie | rel=r_associated | relid=0 | w=20
  753. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ichtyose, affection neurologique spastique, et oligophrénie
    n1=en:deafness, autosomal recessive 1a | n2=ichtyose, affection neurologique spastique, et oligophrénie | rel=r_associated | relid=0 | w=20
  754. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ictère nucléaire
    n1=en:deafness, autosomal recessive 1a | n2=ictère nucléaire | rel=r_associated | relid=0 | w=20
  755. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> idiotie spastique amaurotique axonale
    n1=en:deafness, autosomal recessive 1a | n2=idiotie spastique amaurotique axonale | rel=r_associated | relid=0 | w=20
  756. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> imperforation anale
    n1=en:deafness, autosomal recessive 1a | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  757. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> imperforation de l'anus
    n1=en:deafness, autosomal recessive 1a | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  758. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> inflammation musculaire
    n1=en:deafness, autosomal recessive 1a | n2=inflammation musculaire | rel=r_associated | relid=0 | w=20
  759. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> insensibilité congénitale à la douleur de type III
    n1=en:deafness, autosomal recessive 1a | n2=insensibilité congénitale à la douleur de type III | rel=r_associated | relid=0 | w=20
  760. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:deafness, autosomal recessive 1a | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  761. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Jacobsen (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Jacobsen (syndrome de) | rel=r_associated | relid=0 | w=20
  762. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> lèpre
    n1=en:deafness, autosomal recessive 1a | n2=lèpre | rel=r_associated | relid=0 | w=20
  763. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> léproserie
    n1=en:deafness, autosomal recessive 1a | n2=léproserie | rel=r_associated | relid=0 | w=20
  764. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> leprosy
    n1=en:deafness, autosomal recessive 1a | n2=leprosy | rel=r_associated | relid=0 | w=20
  765. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> leptoméningite tuberculeuse
    n1=en:deafness, autosomal recessive 1a | n2=leptoméningite tuberculeuse | rel=r_associated | relid=0 | w=20
  766. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:deafness, autosomal recessive 1a | n2=leucinose | rel=r_associated | relid=0 | w=20
  767. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> lévocardie
    n1=en:deafness, autosomal recessive 1a | n2=lévocardie | rel=r_associated | relid=0 | w=20
  768. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> lipodystrophie partielle familiale
    n1=en:deafness, autosomal recessive 1a | n2=lipodystrophie partielle familiale | rel=r_associated | relid=0 | w=20
  769. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> lissencéphalie
    n1=en:deafness, autosomal recessive 1a | n2=lissencéphalie | rel=r_associated | relid=0 | w=20
  770. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie à virus de Marburg
    n1=en:deafness, autosomal recessive 1a | n2=maladie à virus de Marburg | rel=r_associated | relid=0 | w=20
  771. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Dercum
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Dercum | rel=r_associated | relid=0 | w=20
  772. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de marfan
    n1=en:deafness, autosomal recessive 1a | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  773. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Perthes
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Perthes | rel=r_associated | relid=0 | w=20
  774. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Seitelberger
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Seitelberger | rel=r_associated | relid=0 | w=20
  775. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de seitelberger
    n1=en:deafness, autosomal recessive 1a | n2=maladie de seitelberger | rel=r_associated | relid=0 | w=20
  776. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:deafness, autosomal recessive 1a | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  777. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  778. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  779. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de Whipple
    n1=en:deafness, autosomal recessive 1a | n2=maladie de Whipple | rel=r_associated | relid=0 | w=20
  780. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Maladie de Whipple
    n1=en:deafness, autosomal recessive 1a | n2=Maladie de Whipple | rel=r_associated | relid=0 | w=20
  781. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie de whipple
    n1=en:deafness, autosomal recessive 1a | n2=maladie de whipple | rel=r_associated | relid=0 | w=20
  782. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie des épiphyses ponctuées
    n1=en:deafness, autosomal recessive 1a | n2=maladie des épiphyses ponctuées | rel=r_associated | relid=0 | w=20
  783. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:deafness, autosomal recessive 1a | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  784. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:deafness, autosomal recessive 1a | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  785. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:deafness, autosomal recessive 1a | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  786. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:deafness, autosomal recessive 1a | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  787. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> maladies des bandes amniotiques
    n1=en:deafness, autosomal recessive 1a | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  788. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> malformation d'Arnold-Chiari
    n1=en:deafness, autosomal recessive 1a | n2=malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  789. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> malformation d'arnold-chiari
    n1=en:deafness, autosomal recessive 1a | n2=malformation d'arnold-chiari | rel=r_associated | relid=0 | w=20
  790. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Malformation d'Arnold-Chiari
    n1=en:deafness, autosomal recessive 1a | n2=Malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  791. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> médecin ORL
    n1=en:deafness, autosomal recessive 1a | n2=médecin ORL | rel=r_associated | relid=0 | w=20
  792. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse
    n1=en:deafness, autosomal recessive 1a | n2=méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  793. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse examen non précisé
    n1=en:deafness, autosomal recessive 1a | n2=méningite tuberculeuse examen non précisé | rel=r_associated | relid=0 | w=20
  794. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> mésentérique supérieure (syndrome de l'artère)
    n1=en:deafness, autosomal recessive 1a | n2=mésentérique supérieure (syndrome de l'artère) | rel=r_associated | relid=0 | w=20
  795. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> microdélétion 5q35
    n1=en:deafness, autosomal recessive 1a | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  796. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> myocardiopathie de tako-tsubo
    n1=en:deafness, autosomal recessive 1a | n2=myocardiopathie de tako-tsubo | rel=r_associated | relid=0 | w=20
  797. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> myokymie
    n1=en:deafness, autosomal recessive 1a | n2=myokymie | rel=r_associated | relid=0 | w=20
  798. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> myosite
    n1=en:deafness, autosomal recessive 1a | n2=myosite | rel=r_associated | relid=0 | w=20
  799. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> myosites
    n1=en:deafness, autosomal recessive 1a | n2=myosites | rel=r_associated | relid=0 | w=20
  800. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> néphrocalcinose
    n1=en:deafness, autosomal recessive 1a | n2=néphrocalcinose | rel=r_associated | relid=0 | w=20
  801. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:deafness, autosomal recessive 1a | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  802. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> neurocysticercose
    n1=en:deafness, autosomal recessive 1a | n2=neurocysticercose | rel=r_associated | relid=0 | w=20
  803. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> neuropathie optique
    n1=en:deafness, autosomal recessive 1a | n2=neuropathie optique | rel=r_associated | relid=0 | w=20
  804. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> nevrilème
    n1=en:deafness, autosomal recessive 1a | n2=nevrilème | rel=r_associated | relid=0 | w=20
  805. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> névrite optique
    n1=en:deafness, autosomal recessive 1a | n2=névrite optique | rel=r_associated | relid=0 | w=20
  806. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> noma
    n1=en:deafness, autosomal recessive 1a | n2=noma | rel=r_associated | relid=0 | w=20
  807. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> odontogénèse imparfaite
    n1=en:deafness, autosomal recessive 1a | n2=odontogénèse imparfaite | rel=r_associated | relid=0 | w=20
  808. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ongles jaunes (syndrome des)
    n1=en:deafness, autosomal recessive 1a | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  809. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose
    n1=en:deafness, autosomal recessive 1a | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  810. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome)
    n1=en:deafness, autosomal recessive 1a | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  811. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasie
    n1=en:deafness, autosomal recessive 1a | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
  812. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasies
    n1=en:deafness, autosomal recessive 1a | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
  813. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ostéopétrose avec acidose rénale tubulaire
    n1=en:deafness, autosomal recessive 1a | n2=ostéopétrose avec acidose rénale tubulaire | rel=r_associated | relid=0 | w=20
  814. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> ostéopoecilie
    n1=en:deafness, autosomal recessive 1a | n2=ostéopoecilie | rel=r_associated | relid=0 | w=20
  815. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> oto-rhino
    n1=en:deafness, autosomal recessive 1a | n2=oto-rhino | rel=r_associated | relid=0 | w=20
  816. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> oto-rhino-laryngologiste
    n1=en:deafness, autosomal recessive 1a | n2=oto-rhino-laryngologiste | rel=r_associated | relid=0 | w=20
  817. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> otorhinolaryngologiste
    n1=en:deafness, autosomal recessive 1a | n2=otorhinolaryngologiste | rel=r_associated | relid=0 | w=20
  818. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> pachyméningite hypertrophique tuberculeuse
    n1=en:deafness, autosomal recessive 1a | n2=pachyméningite hypertrophique tuberculeuse | rel=r_associated | relid=0 | w=20
  819. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> pachyonychie congénitale de Jadassohn-Lewandowsky
    n1=en:deafness, autosomal recessive 1a | n2=pachyonychie congénitale de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  820. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> panencéphalite subaiguë sclérosante
    n1=en:deafness, autosomal recessive 1a | n2=panencéphalite subaiguë sclérosante | rel=r_associated | relid=0 | w=20
  821. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> panuvéite
    n1=en:deafness, autosomal recessive 1a | n2=panuvéite | rel=r_associated | relid=0 | w=20
  822. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> papulose atrophiante maligne de Degos
    n1=en:deafness, autosomal recessive 1a | n2=papulose atrophiante maligne de Degos | rel=r_associated | relid=0 | w=20
  823. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> paragangliome (mise en évidence scintigraphique du)
    n1=en:deafness, autosomal recessive 1a | n2=paragangliome (mise en évidence scintigraphique du) | rel=r_associated | relid=0 | w=20
  824. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> paragonimiase
    n1=en:deafness, autosomal recessive 1a | n2=paragonimiase | rel=r_associated | relid=0 | w=20
  825. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> paragonimose
    n1=en:deafness, autosomal recessive 1a | n2=paragonimose | rel=r_associated | relid=0 | w=20
  826. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> paralysie périodique familiale
    n1=en:deafness, autosomal recessive 1a | n2=paralysie périodique familiale | rel=r_associated | relid=0 | w=20
  827. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> paralysie supranucléaire progressive
    n1=en:deafness, autosomal recessive 1a | n2=paralysie supranucléaire progressive | rel=r_associated | relid=0 | w=20
  828. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> pemphigoïde bénigne des muqueuses
    n1=en:deafness, autosomal recessive 1a | n2=pemphigoïde bénigne des muqueuses | rel=r_associated | relid=0 | w=20
  829. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> peste
    n1=en:deafness, autosomal recessive 1a | n2=peste | rel=r_associated | relid=0 | w=20
  830. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> peste noire
    n1=en:deafness, autosomal recessive 1a | n2=peste noire | rel=r_associated | relid=0 | w=20
  831. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> phacomatose congenitale
    n1=en:deafness, autosomal recessive 1a | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  832. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> piébaldisme
    n1=en:deafness, autosomal recessive 1a | n2=piébaldisme | rel=r_associated | relid=0 | w=20
  833. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> piebaldisme
    n1=en:deafness, autosomal recessive 1a | n2=piebaldisme | rel=r_associated | relid=0 | w=20
  834. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> pityriasis rubra pilaire
    n1=en:deafness, autosomal recessive 1a | n2=pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  835. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Pityriasis rubra pilaire
    n1=en:deafness, autosomal recessive 1a | n2=Pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  836. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Plummer-Vinson (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Plummer-Vinson (syndrome de) | rel=r_associated | relid=0 | w=20
  837. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> porphyrie cutanée tardive
    n1=en:deafness, autosomal recessive 1a | n2=porphyrie cutanée tardive | rel=r_associated | relid=0 | w=20
  838. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> porphyrie érythropoïétique
    n1=en:deafness, autosomal recessive 1a | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  839. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> progeria
    n1=en:deafness, autosomal recessive 1a | n2=progeria | rel=r_associated | relid=0 | w=20
  840. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> progéria
    n1=en:deafness, autosomal recessive 1a | n2=progéria | rel=r_associated | relid=0 | w=20
  841. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> prosopagnosie
    n1=en:deafness, autosomal recessive 1a | n2=prosopagnosie | rel=r_associated | relid=0 | w=20
  842. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> prosopoagnosie
    n1=en:deafness, autosomal recessive 1a | n2=prosopoagnosie | rel=r_associated | relid=0 | w=20
  843. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire
    n1=en:deafness, autosomal recessive 1a | n2=protéinose alvéolaire | rel=r_associated | relid=0 | w=20
  844. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire pulmonaire
    n1=en:deafness, autosomal recessive 1a | n2=protéinose alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
  845. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> protoproporphyrie érythropoïétique
    n1=en:deafness, autosomal recessive 1a | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  846. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> psychose de Korsakoff
    n1=en:deafness, autosomal recessive 1a | n2=psychose de Korsakoff | rel=r_associated | relid=0 | w=20
  847. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> psychose de korsakoff
    n1=en:deafness, autosomal recessive 1a | n2=psychose de korsakoff | rel=r_associated | relid=0 | w=20
  848. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> scléromyxoedème d'Arndt-Gottron
    n1=en:deafness, autosomal recessive 1a | n2=scléromyxoedème d'Arndt-Gottron | rel=r_associated | relid=0 | w=20
  849. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Seitelberger
    n1=en:deafness, autosomal recessive 1a | n2=Seitelberger | rel=r_associated | relid=0 | w=20
  850. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Seitelberger (maladie de)
    n1=en:deafness, autosomal recessive 1a | n2=Seitelberger (maladie de) | rel=r_associated | relid=0 | w=20
  851. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> septo-optic dysplasia
    n1=en:deafness, autosomal recessive 1a | n2=septo-optic dysplasia | rel=r_associated | relid=0 | w=20
  852. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Silver-Russell (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
  853. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:deafness, autosomal recessive 1a | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  854. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> situs inversus
    n1=en:deafness, autosomal recessive 1a | n2=situs inversus | rel=r_associated | relid=0 | w=20
  855. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Sotos (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  856. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> surdité bilatérale totale
    n1=en:deafness, autosomal recessive 1a | n2=surdité bilatérale totale | rel=r_associated | relid=0 | w=20
  857. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> surdité totale
    n1=en:deafness, autosomal recessive 1a | n2=surdité totale | rel=r_associated | relid=0 | w=20
  858. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome cardio-facio-cutané
    n1=en:deafness, autosomal recessive 1a | n2=syndrome cardio-facio-cutané | rel=r_associated | relid=0 | w=20
  859. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome cérébro-oculo-faciosquelettique
    n1=en:deafness, autosomal recessive 1a | n2=syndrome cérébro-oculo-faciosquelettique | rel=r_associated | relid=0 | w=20
  860. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de bride amniotique
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  861. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  862. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de duane
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de duane | rel=r_associated | relid=0 | w=20
  863. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Duane
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Duane | rel=r_associated | relid=0 | w=20
  864. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  865. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de goltz
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
  866. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Goltz
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
  867. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Jacobsen
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
  868. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de jadassohn-lewandowsky
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de jadassohn-lewandowsky | rel=r_associated | relid=0 | w=20
  869. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Jadassohn-Lewandowsky
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  870. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Kelly-Paterson
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Kelly-Paterson | rel=r_associated | relid=0 | w=20
  871. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de marfan
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  872. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  873. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Plummer-Vinson
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  874. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de plummer-vinson
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de plummer-vinson | rel=r_associated | relid=0 | w=20
  875. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Syndrome de Plummer-Vinson
    n1=en:deafness, autosomal recessive 1a | n2=Syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  876. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:deafness, autosomal recessive 1a | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  877. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  878. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  879. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de shy-drager
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de shy-drager | rel=r_associated | relid=0 | w=20
  880. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Syndrome de Shy-Drager
    n1=en:deafness, autosomal recessive 1a | n2=Syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  881. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Shy-Drager
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  882. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Silver-Russell
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
  883. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de silver-russell
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
  884. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de soto
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  885. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Sotos
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  886. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de sotos
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  887. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Stilling-Türk-Duane
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Stilling-Türk-Duane | rel=r_associated | relid=0 | w=20
  888. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de Türk-Stilling-Duane
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de Türk-Stilling-Duane | rel=r_associated | relid=0 | w=20
  889. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome de türk-stilling-duane
    n1=en:deafness, autosomal recessive 1a | n2=syndrome de türk-stilling-duane | rel=r_associated | relid=0 | w=20
  890. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome des brides amniotiques
    n1=en:deafness, autosomal recessive 1a | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  891. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome des histiocytes bleu marine
    n1=en:deafness, autosomal recessive 1a | n2=syndrome des histiocytes bleu marine | rel=r_associated | relid=0 | w=20
  892. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome des yeux de chat
    n1=en:deafness, autosomal recessive 1a | n2=syndrome des yeux de chat | rel=r_associated | relid=0 | w=20
  893. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome hétérotaxique
    n1=en:deafness, autosomal recessive 1a | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
  894. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type 2
    n1=en:deafness, autosomal recessive 1a | n2=syndrome tricho-rhino-phalangien de type 2 | rel=r_associated | relid=0 | w=20
  895. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type ii
    n1=en:deafness, autosomal recessive 1a | n2=syndrome tricho-rhino-phalangien de type ii | rel=r_associated | relid=0 | w=20
  896. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type II
    n1=en:deafness, autosomal recessive 1a | n2=syndrome tricho-rhino-phalangien de type II | rel=r_associated | relid=0 | w=20
  897. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> trachéo-bronchomégalie
    n1=en:deafness, autosomal recessive 1a | n2=trachéo-bronchomégalie | rel=r_associated | relid=0 | w=20
  898. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> trichothiodystrophie
    n1=en:deafness, autosomal recessive 1a | n2=trichothiodystrophie | rel=r_associated | relid=0 | w=20
  899. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> tuberculose des méninges
    n1=en:deafness, autosomal recessive 1a | n2=tuberculose des méninges | rel=r_associated | relid=0 | w=20
  900. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> tuberculose méningée
    n1=en:deafness, autosomal recessive 1a | n2=tuberculose méningée | rel=r_associated | relid=0 | w=20
  901. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Türk-Stilling-Duane (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Türk-Stilling-Duane (syndrome de) | rel=r_associated | relid=0 | w=20
  902. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:deafness, autosomal recessive 1a | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  903. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> wallérienne (dégénérescence)
    n1=en:deafness, autosomal recessive 1a | n2=wallérienne (dégénérescence) | rel=r_associated | relid=0 | w=20
  904. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> Whipple (maladie de)
    n1=en:deafness, autosomal recessive 1a | n2=Whipple (maladie de) | rel=r_associated | relid=0 | w=20
  905. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:deafness, autosomal recessive 1a | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  906. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:deafness, autosomal recessive 1a | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  907. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:deafness, autosomal recessive 1a | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  908. en:deafness, autosomal recessive 1a -- r_associated #0: 20 / 0.465 -> yellow nail syndrome
    n1=en:deafness, autosomal recessive 1a | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
≈ 1332 relations entrantes

  1. peste
    (maladie)
     --- r_associated #0: 494 --> en:deafness, autosomal recessive 1a
    n1=peste
    (maladie)
    | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=494
  2. en:plague --- r_associated #0: 490 --> en:deafness, autosomal recessive 1a
    n1=en:plague | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=490
  3. syndrome de Goltz --- r_associated #0: 407 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Goltz | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=407
  4. hypoplasie dermique focale --- r_associated #0: 406 --> en:deafness, autosomal recessive 1a
    n1=hypoplasie dermique focale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=406
  5. Goltz --- r_associated #0: 404 --> en:deafness, autosomal recessive 1a
    n1=Goltz | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=404
  6. en:focal dermal hypoplasia --- r_associated #0: 395 --> en:deafness, autosomal recessive 1a
    n1=en:focal dermal hypoplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=395
  7. hypoplasie dermique en aires --- r_associated #0: 394 --> en:deafness, autosomal recessive 1a
    n1=hypoplasie dermique en aires | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=394
  8. en:anterior plagiocephalies, synostotic --- r_associated #0: 326 --> en:deafness, autosomal recessive 1a
    n1=en:anterior plagiocephalies, synostotic | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=326
  9. en:congenital deafness --- r_associated #0: 300 --> en:deafness, autosomal recessive 1a
    n1=en:congenital deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=300
  10. surdité congénitale --- r_associated #0: 297 --> en:deafness, autosomal recessive 1a
    n1=surdité congénitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=297
  11. surdité héréditaire --- r_associated #0: 295 --> en:deafness, autosomal recessive 1a
    n1=surdité héréditaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=295
  12. en:marfan syndrome --- r_associated #0: 285 --> en:deafness, autosomal recessive 1a
    n1=en:marfan syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=285
  13. crânio-sténose --- r_associated #0: 283 --> en:deafness, autosomal recessive 1a
    n1=crânio-sténose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=283
  14. en:craniosynostosis --- r_associated #0: 282 --> en:deafness, autosomal recessive 1a
    n1=en:craniosynostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=282
  15. crâniosynostose --- r_associated #0: 281 --> en:deafness, autosomal recessive 1a
    n1=crâniosynostose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=281
  16. maladie de Marfan --- r_associated #0: 281 --> en:deafness, autosomal recessive 1a
    n1=maladie de Marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=281
  17. syndrome de Marfan --- r_associated #0: 281 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=281
  18. craniosynostose --- r_associated #0: 280 --> en:deafness, autosomal recessive 1a
    n1=craniosynostose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=280
  19. arachnodactylie --- r_associated #0: 276 --> en:deafness, autosomal recessive 1a
    n1=arachnodactylie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=276
  20. crâniosténose --- r_associated #0: 276 --> en:deafness, autosomal recessive 1a
    n1=crâniosténose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=276
  21. en:arachnodactyly --- r_associated #0: 255 --> en:deafness, autosomal recessive 1a
    n1=en:arachnodactyly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=255
  22. en:primary progressive aphasia --- r_associated #0: 211 --> en:deafness, autosomal recessive 1a
    n1=en:primary progressive aphasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=211
  23. aphasies primaires progressives --- r_associated #0: 208 --> en:deafness, autosomal recessive 1a
    n1=aphasies primaires progressives | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=208
  24. aphasie primaire progressive --- r_associated #0: 207 --> en:deafness, autosomal recessive 1a
    n1=aphasie primaire progressive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=207
  25. en:sotos syndrome --- r_associated #0: 197 --> en:deafness, autosomal recessive 1a
    n1=en:sotos syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=197
  26. gigantisme cérébral --- r_associated #0: 196 --> en:deafness, autosomal recessive 1a
    n1=gigantisme cérébral | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=196
  27. syndrome de soto --- r_associated #0: 195 --> en:deafness, autosomal recessive 1a
    n1=syndrome de soto | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=195
  28. syndrome de Sotos --- r_associated #0: 190 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Sotos | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=190
  29. en:sensorineural hearing loss --- r_associated #0: 187 --> en:deafness, autosomal recessive 1a
    n1=en:sensorineural hearing loss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=187
  30. craniosténose --- r_associated #0: 185 --> en:deafness, autosomal recessive 1a
    n1=craniosténose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=185
  31. en:Plummer-Vinson syndrome --- r_associated #0: 185 --> en:deafness, autosomal recessive 1a
    n1=en:Plummer-Vinson syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=185
  32. en:sotos' syndrome --- r_associated #0: 185 --> en:deafness, autosomal recessive 1a
    n1=en:sotos' syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=185
  33. perte d'audition sensorineurale --- r_associated #0: 184 --> en:deafness, autosomal recessive 1a
    n1=perte d'audition sensorineurale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=184
  34. en:aortic coarctation --- r_associated #0: 183 --> en:deafness, autosomal recessive 1a
    n1=en:aortic coarctation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=183
  35. en:plummer-vinson syndrome --- r_associated #0: 182 --> en:deafness, autosomal recessive 1a
    n1=en:plummer-vinson syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=182
  36. coarctation aortique --- r_associated #0: 180 --> en:deafness, autosomal recessive 1a
    n1=coarctation aortique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=180
  37. aphasie progressive primaire --- r_associated #0: 177 --> en:deafness, autosomal recessive 1a
    n1=aphasie progressive primaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=177
  38. cysticercose cérébrale --- r_associated #0: 172 --> en:deafness, autosomal recessive 1a
    n1=cysticercose cérébrale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=172
  39. paralysies périodiques familiales --- r_associated #0: 172 --> en:deafness, autosomal recessive 1a
    n1=paralysies périodiques familiales | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=172
  40. en:familial periodic paralysis --- r_associated #0: 171 --> en:deafness, autosomal recessive 1a
    n1=en:familial periodic paralysis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=171
  41. cysticercose du système nerveux central --- r_associated #0: 170 --> en:deafness, autosomal recessive 1a
    n1=cysticercose du système nerveux central | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=170
  42. paralysie périodique familiale --- r_associated #0: 170 --> en:deafness, autosomal recessive 1a
    n1=paralysie périodique familiale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=170
  43. en:neurocysticercosis --- r_associated #0: 162 --> en:deafness, autosomal recessive 1a
    n1=en:neurocysticercosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=162
  44. cysticercose neurologique --- r_associated #0: 161 --> en:deafness, autosomal recessive 1a
    n1=cysticercose neurologique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=161
  45. Weir Mitchell --- r_associated #0: 155 --> en:deafness, autosomal recessive 1a
    n1=Weir Mitchell | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=155
  46. cysticercose --- r_associated #0: 155 --> en:deafness, autosomal recessive 1a
    n1=cysticercose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=155
  47. cysticercoses --- r_associated #0: 155 --> en:deafness, autosomal recessive 1a
    n1=cysticercoses | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=155
  48. en:cysticercosis --- r_associated #0: 155 --> en:deafness, autosomal recessive 1a
    n1=en:cysticercosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=155
  49. neurocysticercose --- r_associated #0: 155 --> en:deafness, autosomal recessive 1a
    n1=neurocysticercose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=155
  50. érythermalgie --- r_associated #0: 148 --> en:deafness, autosomal recessive 1a
    n1=érythermalgie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=148
  51. syndrome de Türk-Stilling-Duane --- r_associated #0: 145 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Türk-Stilling-Duane | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=145
  52. érythromélalgie --- r_associated #0: 145 --> en:deafness, autosomal recessive 1a
    n1=érythromélalgie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=145
  53. en:duane syndrome --- r_associated #0: 144 --> en:deafness, autosomal recessive 1a
    n1=en:duane syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=144
  54. en:erythromelalgia --- r_associated #0: 144 --> en:deafness, autosomal recessive 1a
    n1=en:erythromelalgia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=144
  55. atrophie optique autosomique dominante --- r_associated #0: 141 --> en:deafness, autosomal recessive 1a
    n1=atrophie optique autosomique dominante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=141
  56. syndrome de Duane --- r_associated #0: 141 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Duane | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=141
  57. erythromelalgia --- r_associated #0: 138 --> en:deafness, autosomal recessive 1a
    n1=erythromelalgia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=138
  58. syndrome de duane --- r_associated #0: 134 --> en:deafness, autosomal recessive 1a
    n1=syndrome de duane | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=134
  59. en:sea-blue histiocyte syndrome --- r_associated #0: 131 --> en:deafness, autosomal recessive 1a
    n1=en:sea-blue histiocyte syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=131
  60. syndrome des histiocytes bleu marine --- r_associated #0: 130 --> en:deafness, autosomal recessive 1a
    n1=syndrome des histiocytes bleu marine | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=130
  61. en:whipple disease --- r_associated #0: 126 --> en:deafness, autosomal recessive 1a
    n1=en:whipple disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=126
  62. en:arnold chiari malformation --- r_associated #0: 125 --> en:deafness, autosomal recessive 1a
    n1=en:arnold chiari malformation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=125
  63. maladie de Whipple --- r_associated #0: 125 --> en:deafness, autosomal recessive 1a
    n1=maladie de Whipple | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=125
  64. ostéopétrose avec acidose rénale tubulaire --- r_associated #0: 124 --> en:deafness, autosomal recessive 1a
    n1=ostéopétrose avec acidose rénale tubulaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=124
  65. en:arnold-chiari malformation --- r_associated #0: 121 --> en:deafness, autosomal recessive 1a
    n1=en:arnold-chiari malformation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=121
  66. malformation d'Arnold-Chiari --- r_associated #0: 121 --> en:deafness, autosomal recessive 1a
    n1=malformation d'Arnold-Chiari | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=121
  67. en:osteopetrosis with renal tubular acidosis --- r_associated #0: 120 --> en:deafness, autosomal recessive 1a
    n1=en:osteopetrosis with renal tubular acidosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=120
  68. idiotie spastique amaurotique axonale --- r_associated #0: 119 --> en:deafness, autosomal recessive 1a
    n1=idiotie spastique amaurotique axonale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=119
  69. dystrophie neuroaxonale infantile --- r_associated #0: 117 --> en:deafness, autosomal recessive 1a
    n1=dystrophie neuroaxonale infantile | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=117
  70. démence frontotemporale --- r_associated #0: 115 --> en:deafness, autosomal recessive 1a
    n1=démence frontotemporale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=115
  71. dystrophie neuroaxonale --- r_associated #0: 113 --> en:deafness, autosomal recessive 1a
    n1=dystrophie neuroaxonale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=113
  72. démence fronto-temporale --- r_associated #0: 111 --> en:deafness, autosomal recessive 1a
    n1=démence fronto-temporale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=111
  73. en:osteochondrodysplasia --- r_associated #0: 111 --> en:deafness, autosomal recessive 1a
    n1=en:osteochondrodysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=111
  74. ostéochondrodysplasies --- r_associated #0: 111 --> en:deafness, autosomal recessive 1a
    n1=ostéochondrodysplasies | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=111
  75. en:pyruvate carboxylase deficiency --- r_associated #0: 109 --> en:deafness, autosomal recessive 1a
    n1=en:pyruvate carboxylase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=109
  76. dystrophie neuro-axonale infantile --- r_associated #0: 108 --> en:deafness, autosomal recessive 1a
    n1=dystrophie neuro-axonale infantile | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=108
  77. déficit en pyruvate carboxylase --- r_associated #0: 107 --> en:deafness, autosomal recessive 1a
    n1=déficit en pyruvate carboxylase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=107
  78. anencéphalie --- r_associated #0: 103 --> en:deafness, autosomal recessive 1a
    n1=anencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=103
  79. dystrophie neuroaxonale de Seitelberger --- r_associated #0: 101 --> en:deafness, autosomal recessive 1a
    n1=dystrophie neuroaxonale de Seitelberger | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=101
  80. holoprosencéphalie --- r_associated #0: 101 --> en:deafness, autosomal recessive 1a
    n1=holoprosencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=101
  81. syndrome de Plummer-Vinson --- r_associated #0: 101 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Plummer-Vinson | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=101
  82. syndrome des brides amniotiques --- r_associated #0: 101 --> en:deafness, autosomal recessive 1a
    n1=syndrome des brides amniotiques | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=101
  83. en:frontotemporal dementia --- r_associated #0: 100 --> en:deafness, autosomal recessive 1a
    n1=en:frontotemporal dementia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=100
  84. en:holoprosencephaly --- r_associated #0: 100 --> en:deafness, autosomal recessive 1a
    n1=en:holoprosencephaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=100
  85. en:progressive supranuclear palsy --- r_associated #0: 100 --> en:deafness, autosomal recessive 1a
    n1=en:progressive supranuclear palsy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=100
  86. en:yellow nail syndrome --- r_associated #0: 100 --> en:deafness, autosomal recessive 1a
    n1=en:yellow nail syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=100
  87. syndrome de Rett --- r_associated #0: 100 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Rett | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=100
  88. aïnhum --- r_associated #0: 99 --> en:deafness, autosomal recessive 1a
    n1=aïnhum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=99
  89. en:amniotic band syndrome --- r_associated #0: 99 --> en:deafness, autosomal recessive 1a
    n1=en:amniotic band syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=99
  90. en:anencephaly --- r_associated #0: 99 --> en:deafness, autosomal recessive 1a
    n1=en:anencephaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=99
  91. paralysie supranucléaire progressive --- r_associated #0: 99 --> en:deafness, autosomal recessive 1a
    n1=paralysie supranucléaire progressive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=99
  92. en:piebaldism --- r_associated #0: 98 --> en:deafness, autosomal recessive 1a
    n1=en:piebaldism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=98
  93. en:rett syndrome --- r_associated #0: 98 --> en:deafness, autosomal recessive 1a
    n1=en:rett syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=98
  94. maladies des bandes amniotiques --- r_associated #0: 96 --> en:deafness, autosomal recessive 1a
    n1=maladies des bandes amniotiques | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=96
  95. yellow nail syndrome --- r_associated #0: 96 --> en:deafness, autosomal recessive 1a
    n1=yellow nail syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=96
  96. en:ainhum --- r_associated #0: 95 --> en:deafness, autosomal recessive 1a
    n1=en:ainhum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=95
  97. en:septo-optic dysplasia --- r_associated #0: 95 --> en:deafness, autosomal recessive 1a
    n1=en:septo-optic dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=95
  98. piebaldisme --- r_associated #0: 95 --> en:deafness, autosomal recessive 1a
    n1=piebaldisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=95
  99. piébaldisme --- r_associated #0: 95 --> en:deafness, autosomal recessive 1a
    n1=piébaldisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=95
  100. progeria --- r_associated #0: 95 --> en:deafness, autosomal recessive 1a
    n1=progeria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=95
  101. cataplexie --- r_associated #0: 94 --> en:deafness, autosomal recessive 1a
    n1=cataplexie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=94
  102. en:progeria --- r_associated #0: 94 --> en:deafness, autosomal recessive 1a
    n1=en:progeria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=94
  103. en:cataplexy --- r_associated #0: 93 --> en:deafness, autosomal recessive 1a
    n1=en:cataplexy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=93
  104. ainhum --- r_associated #0: 92 --> en:deafness, autosomal recessive 1a
    n1=ainhum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=92
  105. septo-optic dysplasia --- r_associated #0: 92 --> en:deafness, autosomal recessive 1a
    n1=septo-optic dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=92
  106. syndrome de bride amniotique --- r_associated #0: 91 --> en:deafness, autosomal recessive 1a
    n1=syndrome de bride amniotique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=91
  107. en:jacobsen syndrome --- r_associated #0: 90 --> en:deafness, autosomal recessive 1a
    n1=en:jacobsen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=90
  108. protéinose alvéolaire --- r_associated #0: 90 --> en:deafness, autosomal recessive 1a
    n1=protéinose alvéolaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=90
  109. protéinose alvéolaire pulmonaire --- r_associated #0: 90 --> en:deafness, autosomal recessive 1a
    n1=protéinose alvéolaire pulmonaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=90
  110. maladie de Seitelberger --- r_associated #0: 89 --> en:deafness, autosomal recessive 1a
    n1=maladie de Seitelberger | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=89
  111. Seitelberger --- r_associated #0: 86 --> en:deafness, autosomal recessive 1a
    n1=Seitelberger | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=86
  112. en:pulmonary alveolar proteinosis --- r_associated #0: 86 --> en:deafness, autosomal recessive 1a
    n1=en:pulmonary alveolar proteinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=86
  113. syndrome de Jacobsen --- r_associated #0: 86 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Jacobsen | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=86
  114. leprosy --- r_associated #0: 85 --> en:deafness, autosomal recessive 1a
    n1=leprosy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=85
  115. en:leprosy --- r_associated #0: 84 --> en:deafness, autosomal recessive 1a
    n1=en:leprosy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=84
  116. progéria --- r_associated #0: 84 --> en:deafness, autosomal recessive 1a
    n1=progéria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=84
  117. en:infantile neuroaxonal dystrophy --- r_associated #0: 80 --> en:deafness, autosomal recessive 1a
    n1=en:infantile neuroaxonal dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=80
  118. syndrome de Kelly-Paterson --- r_associated #0: 80 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Kelly-Paterson | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=80
  119. syndrome tricho-rhino-phalangien de type ii --- r_associated #0: 80 --> en:deafness, autosomal recessive 1a
    n1=syndrome tricho-rhino-phalangien de type ii | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=80
  120. en:fragile x syndrome --- r_associated #0: 76 --> en:deafness, autosomal recessive 1a
    n1=en:fragile x syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=76
  121. glaucome capsulaire --- r_associated #0: 76 --> en:deafness, autosomal recessive 1a
    n1=glaucome capsulaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=76
  122. syndrome tricho-rhino-phalangien de type 2 --- r_associated #0: 76 --> en:deafness, autosomal recessive 1a
    n1=syndrome tricho-rhino-phalangien de type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=76
  123. Malformation d'Arnold-Chiari --- r_associated #0: 75 --> en:deafness, autosomal recessive 1a
    n1=Malformation d'Arnold-Chiari | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=75
  124. dystrophies neuroaxonales --- r_associated #0: 75 --> en:deafness, autosomal recessive 1a
    n1=dystrophies neuroaxonales | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=75
  125. en:fragile X syndrome --- r_associated #0: 75 --> en:deafness, autosomal recessive 1a
    n1=en:fragile X syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=75
  126. en:glaucoma capsulare --- r_associated #0: 75 --> en:deafness, autosomal recessive 1a
    n1=en:glaucoma capsulare | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=75
  127. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 74 --> en:deafness, autosomal recessive 1a
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=74
  128. syndrome de türk-stilling-duane --- r_associated #0: 74 --> en:deafness, autosomal recessive 1a
    n1=syndrome de türk-stilling-duane | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=74
  129. en:Whipple disease --- r_associated #0: 73 --> en:deafness, autosomal recessive 1a
    n1=en:Whipple disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=73
  130. déficit en cytochrome oxydase --- r_associated #0: 72 --> en:deafness, autosomal recessive 1a
    n1=déficit en cytochrome oxydase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=72
  131. en:exfoliation syndrome --- r_associated #0: 71 --> en:deafness, autosomal recessive 1a
    n1=en:exfoliation syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=71
  132. syndrome de fragilité du chromosome X --- r_associated #0: 70 --> en:deafness, autosomal recessive 1a
    n1=syndrome de fragilité du chromosome X | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=70
  133. déficit en cytochrome-c oxydase --- r_associated #0: 69 --> en:deafness, autosomal recessive 1a
    n1=déficit en cytochrome-c oxydase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=69
  134. en:cytochrome-c oxidase deficiency --- r_associated #0: 67 --> en:deafness, autosomal recessive 1a
    n1=en:cytochrome-c oxidase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=67
  135. en:erythermalgia --- r_associated #0: 67 --> en:deafness, autosomal recessive 1a
    n1=en:erythermalgia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=67
  136. Syndrome de Rett --- r_associated #0: 65 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Rett | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=65
  137. malformation d'arnold-chiari --- r_associated #0: 65 --> en:deafness, autosomal recessive 1a
    n1=malformation d'arnold-chiari | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=65
  138. situs inversus --- r_associated #0: 62 --> en:deafness, autosomal recessive 1a
    n1=situs inversus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=62
  139. en:Sotos' syndrome --- r_associated #0: 60 --> en:deafness, autosomal recessive 1a
    n1=en:Sotos' syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=60
  140. acromégalie --- r_associated #0: 59 --> en:deafness, autosomal recessive 1a
    n1=acromégalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=59
  141. en:Korsakoff syndrome --- r_associated #0: 59 --> en:deafness, autosomal recessive 1a
    n1=en:Korsakoff syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=59
  142. en:korsakoff syndrome --- r_associated #0: 59 --> en:deafness, autosomal recessive 1a
    n1=en:korsakoff syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=59
  143. en:situs inversus --- r_associated #0: 59 --> en:deafness, autosomal recessive 1a
    n1=en:situs inversus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=59
  144. en:russell-silver syndrome --- r_associated #0: 58 --> en:deafness, autosomal recessive 1a
    n1=en:russell-silver syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=58
  145. syndrome de Silver-Russell --- r_associated #0: 58 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Silver-Russell | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=58
  146. syndrome de silver-russell --- r_associated #0: 58 --> en:deafness, autosomal recessive 1a
    n1=syndrome de silver-russell | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=58
  147. syndrome tricho-rhino-phalangien de type II --- r_associated #0: 58 --> en:deafness, autosomal recessive 1a
    n1=syndrome tricho-rhino-phalangien de type II | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=58
  148. en:acromegaly --- r_associated #0: 56 --> en:deafness, autosomal recessive 1a
    n1=en:acromegaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=56
  149. dystrophies neuro-axonales --- r_associated #0: 55 --> en:deafness, autosomal recessive 1a
    n1=dystrophies neuro-axonales | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=55
  150. en:glutaric acidemia type 1 --- r_associated #0: 55 --> en:deafness, autosomal recessive 1a
    n1=en:glutaric acidemia type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=55
  151. peste --- r_associated #0: 55 --> en:deafness, autosomal recessive 1a
    n1=peste | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=55
  152. syndrome de rett --- r_associated #0: 55 --> en:deafness, autosomal recessive 1a
    n1=syndrome de rett | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=55
  153. acidurie glutarique de type 1 --- r_associated #0: 54 --> en:deafness, autosomal recessive 1a
    n1=acidurie glutarique de type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=54
  154. en:pick's disease --- r_associated #0: 54 --> en:deafness, autosomal recessive 1a
    n1=en:pick's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=54
  155. dysplasie cléidocrânienne --- r_associated #0: 52 --> en:deafness, autosomal recessive 1a
    n1=dysplasie cléidocrânienne | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=52
  156. maladie de marfan --- r_associated #0: 52 --> en:deafness, autosomal recessive 1a
    n1=maladie de marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=52
  157. syndrome de marfan --- r_associated #0: 52 --> en:deafness, autosomal recessive 1a
    n1=syndrome de marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=52
  158. dentine opalescente héréditaire --- r_associated #0: 51 --> en:deafness, autosomal recessive 1a
    n1=dentine opalescente héréditaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=51
  159. en:cardio-facio-cutaneous syndrome --- r_associated #0: 51 --> en:deafness, autosomal recessive 1a
    n1=en:cardio-facio-cutaneous syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=51
  160. trachéo-bronchomégalie --- r_associated #0: 51 --> en:deafness, autosomal recessive 1a
    n1=trachéo-bronchomégalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=51
  161. DentinoGenesis Imperfecta --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=DentinoGenesis Imperfecta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  162. dysplasie cléido-crânienne --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=dysplasie cléido-crânienne | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  163. en:ENT specialist --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=en:ENT specialist | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  164. en:Marfan's syndrome --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=en:Marfan's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  165. en:Pick's disease --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=en:Pick's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  166. en:heterotaxy syndrome --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=en:heterotaxy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  167. en:tracheobronchomegaly --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=en:tracheobronchomegaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  168. hydrops fœtoplacentaire --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=hydrops fœtoplacentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  169. névrite optique --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=névrite optique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  170. oto-rhino --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=oto-rhino | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  171. oto-rhino-laryngologiste --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=oto-rhino-laryngologiste | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  172. surdité totale --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=surdité totale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  173. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:deafness, autosomal recessive 1a
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=50
  174. acidémie glutarique de type 1 --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=acidémie glutarique de type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  175. dentinogenesis imperfecta --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=dentinogenesis imperfecta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  176. en:cardiofaciocutaneous syndrome --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=en:cardiofaciocutaneous syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  177. en:dentinogenesis imperfecta --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=en:dentinogenesis imperfecta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  178. en:nose and throat specialist --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=en:nose and throat specialist | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  179. en:ophthalmoneuritis --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=en:ophthalmoneuritis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  180. en:trichorhinophalangeal syndrome type II --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=en:trichorhinophalangeal syndrome type II | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  181. hydrops foetoplacentaire --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=hydrops foetoplacentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  182. syndrome des yeux de chat --- r_associated #0: 49 --> en:deafness, autosomal recessive 1a
    n1=syndrome des yeux de chat | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=49
  183. acromegaly --- r_associated #0: 48 --> en:deafness, autosomal recessive 1a
    n1=acromegaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=48
  184. en:cat-eye syndrome --- r_associated #0: 47 --> en:deafness, autosomal recessive 1a
    n1=en:cat-eye syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=47
  185. en:chondrodysplasia punctata --- r_associated #0: 47 --> en:deafness, autosomal recessive 1a
    n1=en:chondrodysplasia punctata | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=47
  186. déficience auditive totale --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=déficience auditive totale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  187. en:cerebrotendinous xanthomatosis --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=en:cerebrotendinous xanthomatosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  188. en:optic neuritis --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=en:optic neuritis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  189. otorhinolaryngologiste --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=otorhinolaryngologiste | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  190. pityriasis rubra pilaire --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=pityriasis rubra pilaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  191. syndrome de Jadassohn-Lewandowsky --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Jadassohn-Lewandowsky | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  192. xanthomatose cérébro-tendineuse --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=xanthomatose cérébro-tendineuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  193. xanthomatose cérébrotendineuse --- r_associated #0: 46 --> en:deafness, autosomal recessive 1a
    n1=xanthomatose cérébrotendineuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=46
  194. acrodermatite entéropathique --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=acrodermatite entéropathique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  195. dentinogénèse imparfaite --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=dentinogénèse imparfaite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  196. en:complete deafness --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=en:complete deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  197. intolérance au fructose --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=intolérance au fructose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  198. psychose de korsakoff --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=psychose de korsakoff | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  199. scléromyxœdème d'Arndt-Gottron --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=scléromyxœdème d'Arndt-Gottron | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  200. syndrome de shy-drager --- r_associated #0: 45 --> en:deafness, autosomal recessive 1a
    n1=syndrome de shy-drager | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=45
  201. anasarque foeto-placentaire --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=anasarque foeto-placentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  202. chondrodysplasia punctata --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=chondrodysplasia punctata | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  203. en:acrodermatitis enteropathica --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=en:acrodermatitis enteropathica | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  204. en:pityriasis rubra pilaris --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=en:pityriasis rubra pilaris | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  205. léproserie --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=léproserie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  206. maladie de seitelberger --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=maladie de seitelberger | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  207. syndrome de goltz --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=syndrome de goltz | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  208. syndrome de sotos --- r_associated #0: 44 --> en:deafness, autosomal recessive 1a
    n1=syndrome de sotos | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=44
  209. Syndrome de Shy-Drager --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Shy-Drager | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  210. en:craniofacial dysostosis --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:craniofacial dysostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  211. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  212. en:dyschromatosis symmetrica hereditaria --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:dyschromatosis symmetrica hereditaria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  213. en:fox-fordyce disease --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:fox-fordyce disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  214. en:hereditary fructose intolerance --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary fructose intolerance | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  215. en:hyperkalemic periodic paralysis --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:hyperkalemic periodic paralysis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  216. en:selective antibody deficiency with normal immunoglobulins --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=en:selective antibody deficiency with normal immunoglobulins | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  217. hétérotaxie --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=hétérotaxie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  218. imperforation de l'anus --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=imperforation de l'anus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  219. syndrome de Shy-Drager --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Shy-Drager | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  220. syndrome de douleur extrême paroxystique --- r_associated #0: 43 --> en:deafness, autosomal recessive 1a
    n1=syndrome de douleur extrême paroxystique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=43
  221. Seitelberger (maladie de) --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=Seitelberger (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  222. Syndrome de Plummer-Vinson --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Plummer-Vinson | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  223. en:hearing loss, profound prelingual sensorineural --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=en:hearing loss, profound prelingual sensorineural | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  224. en:levocardia --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=en:levocardia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  225. en:pachyonychia congenita --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=en:pachyonychia congenita | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  226. protoproporphyrie érythropoïétique --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=protoproporphyrie érythropoïétique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  227. scléromyxoedème d'Arndt-Gottron --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=scléromyxoedème d'Arndt-Gottron | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  228. syndrome hétérotaxique --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=syndrome hétérotaxique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  229. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 42 --> en:deafness, autosomal recessive 1a
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=42
  230. Sotos (syndrome de) --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=Sotos (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  231. déficit en protéine trifonctionnelle mitochondriale --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=déficit en protéine trifonctionnelle mitochondriale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  232. en:acatalasemia --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:acatalasemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  233. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  234. en:alveolar proteinosis --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:alveolar proteinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  235. en:codas syndrome --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:codas syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  236. en:empty sella syndrome --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:empty sella syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  237. en:erythropoietic protoporphyria --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:erythropoietic protoporphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  238. en:hereditary deafness --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  239. en:urea cycle metabolism disorder --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=en:urea cycle metabolism disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  240. imperforation anale --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=imperforation anale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  241. ostéochondrodysplasie --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=ostéochondrodysplasie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  242. porphyrie érythropoïétique --- r_associated #0: 41 --> en:deafness, autosomal recessive 1a
    n1=porphyrie érythropoïétique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=41
  243. Whipple (maladie de) --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=Whipple (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  244. anasarque foetoplacentaire --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=anasarque foetoplacentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  245. dysostose craniofaciale --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=dysostose craniofaciale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  246. dysostose crânio-faciale --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=dysostose crânio-faciale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  247. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=dysplasie olfacto-génitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  248. en:Soto's syndrome --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:Soto's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  249. en:black death --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:black death | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  250. en:black plague --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:black plague | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  251. en:cleidocranial dysplasia --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:cleidocranial dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  252. en:erythropoietic porphyria --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:erythropoietic porphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  253. en:heterotaxy --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:heterotaxy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  254. en:hyperpipecolatemia --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:hyperpipecolatemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  255. en:paragonimiasis --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:paragonimiasis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  256. en:paroxysmal extreme pain disorder --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:paroxysmal extreme pain disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  257. en:scleromyxedema --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:scleromyxedema | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  258. en:xxxy and xxxxy syndrome --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=en:xxxy and xxxxy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  259. holoprosencéphalie de type 4 --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=holoprosencéphalie de type 4 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  260. lèpre --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=lèpre | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  261. mésentérique supérieure (syndrome de l'artère) --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=mésentérique supérieure (syndrome de l'artère) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  262. pachyonychie congénitale de Jadassohn-Lewandowsky --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  263. panencéphalite subaiguë sclérosante --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=panencéphalite subaiguë sclérosante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  264. peste noire --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=peste noire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  265. surdité bilatérale totale --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=surdité bilatérale totale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  266. wallérienne (dégénérescence) --- r_associated #0: 40 --> en:deafness, autosomal recessive 1a
    n1=wallérienne (dégénérescence) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=40
  267. Silver-Russell (syndrome de) --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=Silver-Russell (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  268. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  269. dysplasie frontonasale --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=dysplasie frontonasale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  270. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  271. en:Devergie's disease --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:Devergie's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  272. en:ellis-van creveld syndrome --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:ellis-van creveld syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  273. en:gjb2, val84met --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, val84met | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  274. en:hermansky-pudlak syndrome --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:hermansky-pudlak syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  275. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:mitochondrial trifunctional protein deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  276. en:spondyloepimetaphyseal dysplasia with joint laxity type 2 --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  277. en:sudden unexplained infant death --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=en:sudden unexplained infant death | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  278. maladie de whipple --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=maladie de whipple | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  279. maladie à virus de Marburg --- r_associated #0: 39 --> en:deafness, autosomal recessive 1a
    n1=maladie à virus de Marburg | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=39
  280. dysplasie ectodermique --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=dysplasie ectodermique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  281. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  282. en:aniridia --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:aniridia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  283. en:cataplexia --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:cataplexia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  284. en:cataplexis --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:cataplexis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  285. en:congenital pain insensitivity --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:congenital pain insensitivity | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  286. en:hallermann syndrome --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:hallermann syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  287. en:kimura disease --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:kimura disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  288. en:shy-drager syndrome --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:shy-drager syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  289. en:situs mutatus --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=en:situs mutatus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  290. syndrome de Stilling-Türk-Duane --- r_associated #0: 38 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Stilling-Türk-Duane | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=38
  291. Pityriasis rubra pilaire --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=Pityriasis rubra pilaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  292. en:Duane's syndrome --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:Duane's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  293. en:Goltz syndrome --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:Goltz syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  294. en:argininosuccinic aciduria --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:argininosuccinic aciduria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  295. en:cadasil syndrome --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:cadasil syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  296. en:ebstein anomaly --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:ebstein anomaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  297. en:ectodermal dysplasia --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:ectodermal dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  298. en:frontonasal dysplasia --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:frontonasal dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  299. en:imperforate anus --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:imperforate anus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  300. en:norrie syndrome --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:norrie syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  301. en:superior mesenteric artery syndrome --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=en:superior mesenteric artery syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  302. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  303. ichtyose --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=ichtyose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  304. ichtyose folliculaire, atrichie et photophobie --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=ichtyose folliculaire, atrichie et photophobie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  305. ichtyose, affection neurologique spastique, et oligophrénie --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=ichtyose, affection neurologique spastique, et oligophrénie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  306. insensibilité congénitale à la douleur de type III --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=insensibilité congénitale à la douleur de type III | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  307. maladie des épiphyses ponctuées --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=maladie des épiphyses ponctuées | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  308. syndrome de jadassohn-lewandowsky --- r_associated #0: 37 --> en:deafness, autosomal recessive 1a
    n1=syndrome de jadassohn-lewandowsky | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=37
  309. distomatoses pulmonaires --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=distomatoses pulmonaires | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  310. déficit en prolidase --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=déficit en prolidase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  311. en:Black death --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:Black death | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  312. en:ENT doctor --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:ENT doctor | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  313. en:glutaric aciduria, type 1 --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:glutaric aciduria, type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  314. en:kallmann syndrome --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:kallmann syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  315. en:subacute sclerosing panencephalitis --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:subacute sclerosing panencephalitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  316. en:wallerian degeneration --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:wallerian degeneration | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  317. en:x-linked bulbar-muscular atrophy --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=en:x-linked bulbar-muscular atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  318. ichthyose --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=ichthyose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  319. myocardiopathie de tako-tsubo --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=myocardiopathie de tako-tsubo | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  320. neuropathie optique --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=neuropathie optique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  321. nevrilème --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=nevrilème | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  322. prosopagnosie --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=prosopagnosie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  323. prosopoagnosie --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=prosopoagnosie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  324. sirop d'érable (urine à odeur de) --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=sirop d'érable (urine à odeur de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  325. surdité des deux oreilles --- r_associated #0: 36 --> en:deafness, autosomal recessive 1a
    n1=surdité des deux oreilles | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=36
  326. arthrogrypose --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=arthrogrypose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  327. déficit en céto-acide décarboxylase --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=déficit en céto-acide décarboxylase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  328. en:Tay-Sachs disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:Tay-Sachs disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  329. en:achard syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:achard syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  330. en:acrodermatitis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:acrodermatitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  331. en:arthrogryposis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:arthrogryposis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  332. en:autosomal recessive inheritance --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:autosomal recessive inheritance | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  333. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  334. en:cerebral tuberculosis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:cerebral tuberculosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  335. en:cerebrooculofacioskeletal syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:cerebrooculofacioskeletal syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  336. en:choroideremia --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:choroideremia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  337. en:classical maple syrup urine disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:classical maple syrup urine disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  338. en:congenital cortical hyperostosis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:congenital cortical hyperostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  339. en:congenital structural myopathy --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:congenital structural myopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  340. en:deaf-blind disorders --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:deaf-blind disorders | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  341. en:deafness, digenic, gjb2/gjb6 (disorder) --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:deafness, digenic, gjb2/gjb6 (disorder) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  342. en:drug- and toxin-induced pulmonary arterial hypertension --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  343. en:familial partial lipodystrophy --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:familial partial lipodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  344. en:gjb2, arg143trp --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, arg143trp | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  345. en:gjb2, glu118del --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, glu118del | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  346. en:gjb2, trp24ter --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, trp24ter | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  347. en:glanzmann thrombasthenia --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:glanzmann thrombasthenia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  348. en:griscelli syndrome type 2 --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:griscelli syndrome type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  349. en:hard skin syndrome parana type --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:hard skin syndrome parana type | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  350. en:holt-oram syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:holt-oram syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  351. en:hydrops fetalis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:hydrops fetalis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  352. en:kleine-levin syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:kleine-levin syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  353. en:leopard syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:leopard syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  354. en:lesch-nyhan syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:lesch-nyhan syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  355. en:lissencephaly --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:lissencephaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  356. en:malignant hyperthermia syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:malignant hyperthermia syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  357. en:maple syrup urine disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:maple syrup urine disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  358. en:marburg virus disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:marburg virus disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  359. en:melas syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:melas syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  360. en:meningeal tuberculosis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:meningeal tuberculosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  361. en:menkes disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:menkes disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  362. en:multicentric osteolysis, nodulosis, and arthropathy --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:multicentric osteolysis, nodulosis, and arthropathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  363. en:panuveitis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:panuveitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  364. en:pearson marrow-pancreas syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:pearson marrow-pancreas syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  365. en:pelizaeus-merzbacher disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:pelizaeus-merzbacher disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  366. en:rhizomelic dysplasia --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:rhizomelic dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  367. en:rieger syndrome type 1 --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:rieger syndrome type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  368. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  369. en:shprintzen-goldberg craniosynostosis syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  370. en:sudden unexplained death in childhood --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:sudden unexplained death in childhood | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  371. en:tay-sachs disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:tay-sachs disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  372. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  373. en:togaviridae infection --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:togaviridae infection | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  374. en:tuberculosis of meninges (cerebral)(spinal) --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  375. en:tuberculosis, meningeal --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:tuberculosis, meningeal | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  376. en:tuberculous hypertrophic pachymeningitides --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:tuberculous hypertrophic pachymeningitides | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  377. en:tuberculous leptomeningitis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:tuberculous leptomeningitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  378. en:waardenburg syndrome --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:waardenburg syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  379. en:wegener granulomatosis --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:wegener granulomatosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  380. en:x-linked dominant hypophosphatemic rickets --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=en:x-linked dominant hypophosphatemic rickets | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  381. examen non précisé, méningite tuberculeuse --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=examen non précisé, méningite tuberculeuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  382. hérédité autosomale récessive --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=hérédité autosomale récessive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  383. leptoméningite tuberculeuse --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=leptoméningite tuberculeuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  384. leucinose --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=leucinose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  385. lissencéphalie --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=lissencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  386. maladie de Perthes --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie de Perthes | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  387. maladie de Tay-sachs --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie de Tay-sachs | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  388. maladie de tay-sachs --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie de tay-sachs | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  389. maladie des urines avec odeur de sirop erable --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie des urines avec odeur de sirop erable | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  390. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  391. maladie du sirop d'érable --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=maladie du sirop d'érable | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  392. méningite tuberculeuse --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=méningite tuberculeuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  393. méningite tuberculeuse examen non précisé --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=méningite tuberculeuse examen non précisé | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  394. onycho-ostéodysostose --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=onycho-ostéodysostose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  395. pachyméningite hypertrophique tuberculeuse --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=pachyméningite hypertrophique tuberculeuse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  396. syndrome cérébro-oculo-faciosquelettique --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=syndrome cérébro-oculo-faciosquelettique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  397. syndrome de plummer-vinson --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=syndrome de plummer-vinson | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  398. trachéobronchomégalie --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=trachéobronchomégalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  399. tuberculose des méninges --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=tuberculose des méninges | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  400. tuberculose méningée --- r_associated #0: 35 --> en:deafness, autosomal recessive 1a
    n1=tuberculose méningée | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=35
  401. dystrophie orbitaire congénitale --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=dystrophie orbitaire congénitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  402. ectrodactylie --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=ectrodactylie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  403. en:17q21 microdeletion syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:17q21 microdeletion syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  404. en:Gray platelet syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:Gray platelet syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  405. en:Williams syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:Williams syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  406. en:aicardi syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:aicardi syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  407. en:campomelic dysplasia --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:campomelic dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  408. en:carbohydrate-deficient glycoprotein syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:carbohydrate-deficient glycoprotein syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  409. en:cogan-reese syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:cogan-reese syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  410. en:complex regional pain syndrome i --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:complex regional pain syndrome i | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  411. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  412. en:congenital bilateral aplasia of the vas deferens --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:congenital bilateral aplasia of the vas deferens | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  413. en:cryptophthalmos syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:cryptophthalmos syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  414. en:deletion 18q syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:deletion 18q syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  415. en:dextrocardia --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:dextrocardia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  416. en:donohue syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:donohue syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  417. en:ear --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:ear | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  418. en:friedreich ataxia --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:friedreich ataxia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  419. en:gray platelet syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:gray platelet syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  420. en:hereditary angioedema --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary angioedema | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  421. en:ichthyosis --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:ichthyosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  422. en:leucinosis --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:leucinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  423. en:liddle syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:liddle syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  424. en:malignant atrophic papulosis --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:malignant atrophic papulosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  425. en:papillon-lefevre syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:papillon-lefevre syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  426. en:perthes disease --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:perthes disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  427. en:potocki-shaffer syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:potocki-shaffer syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  428. en:progressive bulbar palsy --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:progressive bulbar palsy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  429. en:prolidase deficiency --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:prolidase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  430. en:sjogren-larsson syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:sjogren-larsson syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  431. en:smith-magenis syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:smith-magenis syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  432. en:synpolydactyly --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:synpolydactyly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  433. en:vitelliform macular dystrophy --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:vitelliform macular dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  434. en:williams syndrome --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=en:williams syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  435. holoprosencéphalie de type 2 --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=holoprosencéphalie de type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  436. ongles jaunes (syndrome des) --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=ongles jaunes (syndrome des) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  437. papulose atrophiante maligne de Degos --- r_associated #0: 34 --> en:deafness, autosomal recessive 1a
    n1=papulose atrophiante maligne de Degos | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=34
  438. en:Marfan's disease --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:Marfan's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  439. en:arnold-chiari deformity --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:arnold-chiari deformity | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  440. en:cerebral gigantism --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:cerebral gigantism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  441. en:familial dysautonomia --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:familial dysautonomia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  442. en:myositis --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:myositis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  443. en:nail-patella syndrome --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:nail-patella syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  444. en:neurological cysticercosis --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:neurological cysticercosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  445. en:takotsubo cardiomyopathy --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=en:takotsubo cardiomyopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  446. hydroa vacciniforme de Bazin --- r_associated #0: 33 --> en:deafness, autosomal recessive 1a
    n1=hydroa vacciniforme de Bazin | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=33
  447. en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  448. en:alpha thalassemia x-linked mental retardation syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  449. en:atrophic muscular disorder --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:atrophic muscular disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  450. en:autoimmune polyendocrinopathy syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:autoimmune polyendocrinopathy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  451. en:caroli disease --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:caroli disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  452. en:cranioectodermal dysplasia --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:cranioectodermal dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  453. en:d-bifunctional protein deficiency --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:d-bifunctional protein deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  454. en:deafness, autosomal recessive 28 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:deafness, autosomal recessive 28 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  455. en:deafness, autosomal recessive 49 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:deafness, autosomal recessive 49 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  456. en:factor v leiden --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:factor v leiden | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  457. en:familial hypertrophic cardiomyopathy --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:familial hypertrophic cardiomyopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  458. en:feingold syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:feingold syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  459. en:generalized arterial calcification of infancy 1 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:generalized arterial calcification of infancy 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  460. en:gjb2, -3438c-t --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, -3438c-t | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  461. en:gjb2, 5-bp dup, nt280 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 5-bp dup, nt280 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  462. en:gjb2, ivs1ds, g-a, +1 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, ivs1ds, g-a, +1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  463. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  464. en:hereditary persistence of fetal hemoglobin --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary persistence of fetal hemoglobin | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  465. en:lysinuric protein intolerance --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:lysinuric protein intolerance | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  466. en:mallory-weiss syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:mallory-weiss syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  467. en:maple-tree syrup disease --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:maple-tree syrup disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  468. en:marshall syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:marshall syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  469. en:prosopagnosia --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:prosopagnosia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  470. en:situs inversus viscerum --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:situs inversus viscerum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  471. en:treacher collins syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:treacher collins syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  472. en:trigger finger disorder --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:trigger finger disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  473. en:uveomeningoencephalitic syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:uveomeningoencephalitic syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  474. en:weaver syndrome --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=en:weaver syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  475. holoprosencéphalie de type 3 --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=holoprosencéphalie de type 3 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  476. noma --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=noma | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  477. phacomatose congenitale --- r_associated #0: 32 --> en:deafness, autosomal recessive 1a
    n1=phacomatose congenitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=32
  478. Plummer-Vinson (syndrome de) --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=Plummer-Vinson (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  479. Syndrome de Marfan --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  480. Türk-Stilling-Duane (syndrome de) --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=Türk-Stilling-Duane (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  481. anasarque --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=anasarque | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  482. anomalie d'Ebstein --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=anomalie d'Ebstein | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  483. dextrocardie --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=dextrocardie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  484. dysostose crâniofaciale --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=dysostose crâniofaciale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  485. dysplasie campomélique --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=dysplasie campomélique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  486. dysérythropoïèse congénitale --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=dysérythropoïèse congénitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  487. en:allgrove syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:allgrove syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  488. en:berardinelli-seip congenital lipodystrophy --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:berardinelli-seip congenital lipodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  489. en:chilblains --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:chilblains | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  490. en:chromosome 2q37 deletion syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:chromosome 2q37 deletion syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  491. en:ectrodactyly --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:ectrodactyly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  492. en:fatal familial insomnia --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:fatal familial insomnia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  493. en:fibrodysplasia ossificans progressiva --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:fibrodysplasia ossificans progressiva | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  494. en:gangrenous stomatitis --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:gangrenous stomatitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  495. en:glycogen storage disease --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:glycogen storage disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  496. en:head and neck --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:head and neck | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  497. en:hereditary orotic aciduria --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary orotic aciduria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  498. en:idiopathic hypersomnolence --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:idiopathic hypersomnolence | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  499. en:iridocorneal endothelial syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:iridocorneal endothelial syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  500. en:jackson-weiss syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:jackson-weiss syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  501. en:kearns-sayre syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:kearns-sayre syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  502. en:kshv inflammatory cytokine syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:kshv inflammatory cytokine syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  503. en:low frequency hearing loss --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:low frequency hearing loss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  504. en:lysosomal storage disease --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:lysosomal storage disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  505. en:myotonic disorder --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:myotonic disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  506. en:pelger-huet anomaly --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:pelger-huet anomaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  507. en:porphyria cutanea tarda --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:porphyria cutanea tarda | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  508. en:pseudoachondroplasia --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:pseudoachondroplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  509. en:pseudotrisomy 13 syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  510. en:triploidy syndrome --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:triploidy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  511. en:tuberculous meningitis --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:tuberculous meningitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  512. en:xerophthalmia --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=en:xerophthalmia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  513. holoprosencéphalie familiale alobaire de type 1 --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  514. lipodystrophie partielle familiale --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=lipodystrophie partielle familiale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  515. lévocardie --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=lévocardie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  516. maladie lysosomique de surcharge --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=maladie lysosomique de surcharge | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  517. malformation d'Ebstein --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=malformation d'Ebstein | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  518. myosite --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=myosite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  519. myosites --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=myosites | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  520. néphrocalcinose --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=néphrocalcinose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  521. onycho-patellaire (syndrome) --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=onycho-patellaire (syndrome) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  522. ostéopoecilie --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=ostéopoecilie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  523. panuvéite --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=panuvéite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  524. paragonimiase --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=paragonimiase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  525. paragonimose --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=paragonimose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  526. pemphigoïde bénigne des muqueuses --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=pemphigoïde bénigne des muqueuses | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  527. porphyrie cutanée tardive --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=porphyrie cutanée tardive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  528. syndrome de Martin-Bell --- r_associated #0: 31 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Martin-Bell | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  529. Duane (syndrome de) --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=Duane (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  530. Goltz (syndrome de) --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=Goltz (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  531. anasarque fœtoplacentaire --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=anasarque fœtoplacentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  532. anasarque foetal --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=anasarque foetal | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  533. déficit en biotinidase --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=déficit en biotinidase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  534. en:22q telomere deletion syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:22q telomere deletion syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  535. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  536. en:CDA --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:CDA | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  537. en:Dercum's disease --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:Dercum's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  538. en:Donohue syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:Donohue syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  539. en:Seitelberger's neuroaxonal dystrophy --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:Seitelberger's neuroaxonal dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  540. en:achondrogenesis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:achondrogenesis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  541. en:adiposis dolorosa --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:adiposis dolorosa | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  542. en:anacusia --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:anacusia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  543. en:brain iron accumulation type i syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:brain iron accumulation type i syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  544. en:branched-chain ketoaciduria --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:branched-chain ketoaciduria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  545. en:coffin-lowry syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:coffin-lowry syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  546. en:deafness, autosomal recessive 1a (disorder) --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:deafness, autosomal recessive 1a (disorder) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  547. en:gjb2, 1-bp del, 35g (dbsnp rs80338939) --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 1-bp del, 35g (dbsnp rs80338939) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  548. en:gjb2, val37ile --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, val37ile | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  549. en:hereditary hyperbilirubinemia --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary hyperbilirubinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  550. en:hydroa vacciniforme --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:hydroa vacciniforme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  551. en:hydrops foetalis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:hydrops foetalis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  552. en:hymenolepiasis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:hymenolepiasis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  553. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  554. en:leper colony --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:leper colony | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  555. en:leprosarium --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:leprosarium | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  556. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  557. en:methionine adenosyltransferase deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:methionine adenosyltransferase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  558. en:myhre syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:myhre syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  559. en:n-acetylglutamate synthase deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:n-acetylglutamate synthase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  560. en:neonatal progeroid syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:neonatal progeroid syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  561. en:neural tube defect --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:neural tube defect | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  562. en:neuroacanthocytosis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:neuroacanthocytosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  563. en:odontogenesis imperfecta --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:odontogenesis imperfecta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  564. en:oeis complex --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:oeis complex | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  565. en:other specified forms of deafness --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:other specified forms of deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  566. en:pentalogy of cantrell --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:pentalogy of cantrell | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  567. en:peritoneal panniculitis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:peritoneal panniculitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  568. en:primary carnitine deficiency --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:primary carnitine deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  569. en:prune belly syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:prune belly syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  570. en:pseudotumor cerebri --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:pseudotumor cerebri | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  571. en:thyroid dysgenesis --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:thyroid dysgenesis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  572. en:thyroid hormone resistance syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:thyroid hormone resistance syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  573. en:waterhouse-friderichsen syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:waterhouse-friderichsen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  574. en:xyy syndrome --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=en:xyy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  575. hydroa vacciniforme --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=hydroa vacciniforme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  576. inflammation musculaire --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=inflammation musculaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  577. maladie de Dercum --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=maladie de Dercum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  578. maladie de Tay-Sachs --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=maladie de Tay-Sachs | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  579. médecin ORL --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=médecin ORL | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  580. neuro-acanthocytose --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=neuro-acanthocytose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  581. odontogénèse imparfaite --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=odontogénèse imparfaite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  582. syndrome sapho --- r_associated #0: 30 --> en:deafness, autosomal recessive 1a
    n1=syndrome sapho | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  583. FMD --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=FMD | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  584. Maladie de Whipple --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=Maladie de Whipple | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  585. aplasie de la paroi abdominale --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=aplasie de la paroi abdominale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  586. en:Martin-Bell's syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:Martin-Bell's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  587. en:Waterhouse-Friderichsen syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:Waterhouse-Friderichsen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  588. en:acrocallosal syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:acrocallosal syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  589. en:anal imperforation --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:anal imperforation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  590. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  591. en:argininemia --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:argininemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  592. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  593. en:atransferrinemia --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:atransferrinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  594. en:autosomal dominant congenital deafness with onychodystrophy --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  595. en:beta-methylcrotonylglycinuria --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:beta-methylcrotonylglycinuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  596. en:coloboma and anal atresia syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:coloboma and anal atresia syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  597. en:combined lipase deficiency --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:combined lipase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  598. en:connexin 26 gene anomaly --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:connexin 26 gene anomaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  599. en:darier disease --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:darier disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  600. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  601. en:episodic pain syndrome, familial, 3 --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:episodic pain syndrome, familial, 3 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  602. en:gjb2, 1-bp del, 167t --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 1-bp del, 167t | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  603. en:gjb2, 1-bp del, 235c --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 1-bp del, 235c | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  604. en:gjb2, gly45glu --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, gly45glu | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  605. en:gjb2, val84leu --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, val84leu | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  606. en:goldenhar syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:goldenhar syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  607. en:hartnup disease --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:hartnup disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  608. en:jervell and lange nielsen syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:jervell and lange nielsen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  609. en:kernicterus --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:kernicterus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  610. en:leri-weill dyschondrosteosis --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:leri-weill dyschondrosteosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  611. en:meckel-gruber syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:meckel-gruber syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  612. en:mitochondrial neurogastrointestingal encephalopathy --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:mitochondrial neurogastrointestingal encephalopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  613. en:mobius syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:mobius syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  614. en:mowat-wilson syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:mowat-wilson syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  615. en:nelson syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:nelson syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  616. en:neuropathy, hereditary sensory and autonomic, type vii --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:neuropathy, hereditary sensory and autonomic, type vii | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  617. en:ossification of posterior longitudinal ligament --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:ossification of posterior longitudinal ligament | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  618. en:pain agnosia --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:pain agnosia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  619. en:sarcitis --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:sarcitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  620. en:short stature homeobox deficiency --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:short stature homeobox deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  621. en:surfactant protein deficiency --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:surfactant protein deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  622. en:trichothiodystrophy --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:trichothiodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  623. en:wolfram syndrome --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=en:wolfram syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  624. ictère nucléaire --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=ictère nucléaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  625. microdélétion 5q35 --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=microdélétion 5q35 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  626. syndrome cardio-facio-cutané --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=syndrome cardio-facio-cutané | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  627. trichothiodystrophie --- r_associated #0: 29 --> en:deafness, autosomal recessive 1a
    n1=trichothiodystrophie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=29
  628. acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  629. agnosie --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=agnosie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  630. analbuminémie --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=analbuminémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  631. chondrodysplasie léthale avec brièveté des côtes --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=chondrodysplasie léthale avec brièveté des côtes | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  632. en:FPLD --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:FPLD | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  633. en:Feingold syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:Feingold syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  634. en:agnosia --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:agnosia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  635. en:analbuminemia --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:analbuminemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  636. en:autosomal dominant optic atrophy --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:autosomal dominant optic atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  637. en:charge syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:charge syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  638. en:congenital disorder of deglycosylation --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:congenital disorder of deglycosylation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  639. en:congenital dyserythropoietic anemia --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:congenital dyserythropoietic anemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  640. en:deafness, digenic, gjb2/gjb3 (disorder) --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:deafness, digenic, gjb2/gjb3 (disorder) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  641. en:erythropoietic uroporphyria --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:erythropoietic uroporphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  642. en:gerstmann-straussler-scheinker disease --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:gerstmann-straussler-scheinker disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  643. en:gjb2, glu47ter --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, glu47ter | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  644. en:holmes-adie syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:holmes-adie syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  645. en:kabuki syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:kabuki syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  646. en:leigh disease --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:leigh disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  647. en:leprosary --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:leprosary | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  648. en:lig4 syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:lig4 syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  649. en:meesmann corneal dystrophy --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:meesmann corneal dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  650. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  651. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  652. en:neuronal intranuclear inclusion disease --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:neuronal intranuclear inclusion disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  653. en:osteopoecilia --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:osteopoecilia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  654. en:osteopoikilosis --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:osteopoikilosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  655. en:pettigrew syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:pettigrew syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  656. en:short rib-polydactyly syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:short rib-polydactyly syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  657. en:stargardt disease --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:stargardt disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  658. en:tolosa-hunt syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:tolosa-hunt syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  659. en:variegate porphyria --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:variegate porphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  660. en:west syndrome --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=en:west syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  661. esgourde --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=esgourde | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  662. psychose de Korsakoff --- r_associated #0: 28 --> en:deafness, autosomal recessive 1a
    n1=psychose de Korsakoff | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=28
  663. albinisme --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=albinisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  664. aniridie, microcornée et cataracte régressive --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=aniridie, microcornée et cataracte régressive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  665. en:Fox-Fordyce disease --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:Fox-Fordyce disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  666. en:Hebra's pityriasis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:Hebra's pityriasis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  667. en:albinism --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:albinism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  668. en:alkaptonuria --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:alkaptonuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  669. en:allan-herndon-dudley syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:allan-herndon-dudley syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  670. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  671. en:arachnodactily --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:arachnodactily | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  672. en:arakawa syndrome ii --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:arakawa syndrome ii | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  673. en:benign mucous membrane pemphigoid --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:benign mucous membrane pemphigoid | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  674. en:biotinidase deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:biotinidase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  675. en:calciphylaxis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:calciphylaxis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  676. en:carnitine palmitoyltransferase i deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:carnitine palmitoyltransferase i deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  677. en:complex regional pain syndrome ii --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:complex regional pain syndrome ii | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  678. en:congenital fiber-type disproportion --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:congenital fiber-type disproportion | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  679. en:dactylolysis spontanea --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:dactylolysis spontanea | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  680. en:digenic dominant --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:digenic dominant | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  681. en:farber lipogranulomatosis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:farber lipogranulomatosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  682. en:gjb2, 12-bp del, 1-bp ins, nt51 --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 12-bp del, 1-bp ins, nt51 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  683. en:gjb2, 14-bp del, nt313 --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, 14-bp del, nt313 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  684. en:gjb2, trp77arg --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, trp77arg | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  685. en:hansenarium --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hansenarium | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  686. en:hantavirus pulmonary syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hantavirus pulmonary syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  687. en:hereditary coproporphyria --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary coproporphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  688. en:hereditary mucosal leukokeratosis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary mucosal leukokeratosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  689. en:heritable pulmonary arterial hypertension --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:heritable pulmonary arterial hypertension | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  690. en:hmg-coa lyase deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hmg-coa lyase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  691. en:hyaline membrane syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:hyaline membrane syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  692. en:immunodeficiency with hyper-igm type 2 --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:immunodeficiency with hyper-igm type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  693. en:juvenile x-linked retinoschisis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:juvenile x-linked retinoschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  694. en:lazar-house --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:lazar-house | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  695. en:mullerian inhibiting factor deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:mullerian inhibiting factor deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  696. en:nephrocalcinosis --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:nephrocalcinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  697. en:neurotoxicity syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:neurotoxicity syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  698. en:non-trisomic autosomal aneuploidy --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:non-trisomic autosomal aneuploidy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  699. en:other specified hearing loss --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:other specified hearing loss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  700. en:otorhinolaryngologist --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:otorhinolaryngologist | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  701. en:persistent fetal circulation --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:persistent fetal circulation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  702. en:pierre robin syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:pierre robin syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  703. en:poland syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:poland syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  704. en:roberts syndrome --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:roberts syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  705. en:thrombocytopenia 2 --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:thrombocytopenia 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  706. en:trisomy 14 mosaicism --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:trisomy 14 mosaicism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  707. en:vestibular dysfunction (in some patients) --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:vestibular dysfunction (in some patients) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  708. en:x-linked creatine transporter deficiency --- r_associated #0: 27 --> en:deafness, autosomal recessive 1a
    n1=en:x-linked creatine transporter deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=27
  709. Jacobsen (syndrome de) --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=Jacobsen (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  710. albinisme oculocutané de type mutant jaune --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=albinisme oculocutané de type mutant jaune | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  711. en:acquired hyperostosis syndrome --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:acquired hyperostosis syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  712. en:albright's hereditary osteodystrophy --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:albright's hereditary osteodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  713. en:anacusis --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:anacusis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  714. en:and mental retardation --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:and mental retardation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  715. en:auditory perceptual disorder --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:auditory perceptual disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  716. en:autosomal recessive hypohidrotic ectodermal dysplasia --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:autosomal recessive hypohidrotic ectodermal dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  717. en:bernard-soulier syndrome --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:bernard-soulier syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  718. en:cleft lip and palate --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:cleft lip and palate | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  719. en:d-glyceric aciduria --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:d-glyceric aciduria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  720. en:deletion 18p syndrome --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:deletion 18p syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  721. en:gitelman syndrome --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:gitelman syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  722. en:gjb2, arg184pro --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, arg184pro | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  723. en:gjb2, asp159val --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, asp159val | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  724. en:gjb2, trp77ter --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, trp77ter | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  725. en:glutaric aciduria type 1 --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:glutaric aciduria type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  726. en:hearing impaired persons --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:hearing impaired persons | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  727. en:high molecular weight kininogen deficiency --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:high molecular weight kininogen deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  728. en:holocarboxylase synthetase deficiency --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:holocarboxylase synthetase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  729. en:hyperlysinemia --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:hyperlysinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  730. en:ichthyosis vera --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:ichthyosis vera | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  731. en:myokymia --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:myokymia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  732. en:orofacial cleft 1 --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:orofacial cleft 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  733. en:orofaciodigital syndrome type 6 --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:orofaciodigital syndrome type 6 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  734. en:pyruvate dehydrogenase deficiency --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:pyruvate dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  735. en:robinow syndrome --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:robinow syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  736. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  737. en:transposition of great vessels --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=en:transposition of great vessels | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  738. myokymie --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=myokymie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  739. paragangliome (mise en évidence scintigraphique du) --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=paragangliome (mise en évidence scintigraphique du) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  740. syndrome de la selle turcique vide --- r_associated #0: 26 --> en:deafness, autosomal recessive 1a
    n1=syndrome de la selle turcique vide | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=26
  741. Hölmgren (triade de) --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=Hölmgren (triade de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  742. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=albinisme avec pigmentation minime | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  743. anacousie --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=anacousie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  744. aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  745. brides amniotiques (syndrome des) --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=brides amniotiques (syndrome des) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  746. dysplasie olfactogénitale --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=dysplasie olfactogénitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  747. déficit congénital en mégacaryocytes --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=déficit congénital en mégacaryocytes | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  748. en:Seitelberger's disease --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=en:Seitelberger's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  749. en:cysticercal disease --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=en:cysticercal disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  750. en:hypopituitarism --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=en:hypopituitarism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  751. en:marfan's syndrome --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=en:marfan's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  752. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=hypogonadisme avec anosmie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  753. hypopituitarisme --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=hypopituitarisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  754. selle turcique vide --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=selle turcique vide | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  755. syndrome de Williams --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Williams | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  756. syndrome de membrane hyaline --- r_associated #0: 25 --> en:deafness, autosomal recessive 1a
    n1=syndrome de membrane hyaline | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=25
  757. acatalasémie --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=acatalasémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  758. acrodermatitis enteropathica --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=acrodermatitis enteropathica | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  759. atransferrinémie --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=atransferrinémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  760. en:Gitelman syndrome --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:Gitelman syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  761. en:Marburg virus disease --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:Marburg virus disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  762. en:chondrodystrophia punctata --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:chondrodystrophia punctata | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  763. en:craniostenosis --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:craniostenosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  764. en:escalope --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:escalope | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  765. en:hand and foot deformity --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:hand and foot deformity | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  766. en:hypothalamic hamartoblastoma --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:hypothalamic hamartoblastoma | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  767. en:onychoosteodysostosis --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=en:onychoosteodysostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  768. glycogénose --- r_associated #0: 24 --> en:deafness, autosomal recessive 1a
    n1=glycogénose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=24
  769. Seitelberger (dystrophie neuroaxonale de) --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=Seitelberger (dystrophie neuroaxonale de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  770. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  771. en:Degos's syndrome --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:Degos's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  772. en:Stargardt disease --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:Stargardt disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  773. en:cutlet --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:cutlet | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  774. en:cysticercus disease --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:cysticercus disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  775. en:fish skin disease --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:fish skin disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  776. en:myitis --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:myitis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  777. en:otolaryngologist --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:otolaryngologist | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  778. en:zinc-deficiency type --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=en:zinc-deficiency type | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  779. hémicéphalie --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=hémicéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  780. maladie de dercum --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=maladie de dercum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  781. xanthique (lithiase) --- r_associated #0: 23 --> en:deafness, autosomal recessive 1a
    n1=xanthique (lithiase) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=23
  782. aniridie, ataxie cérébelleuse et déficience mentale --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=aniridie, ataxie cérébelleuse et déficience mentale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  783. cétoacidurie à chaînes ramifiées --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=cétoacidurie à chaînes ramifiées | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  784. en:Günther's disease --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:Günther's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  785. en:Köbberling's syndrome --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:Köbberling's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  786. en:Wegener granulomatosis --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:Wegener granulomatosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  787. en:anasarca --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:anasarca | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  788. en:proctatresia --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:proctatresia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  789. en:xerophtalmy --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=en:xerophtalmy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  790. porphyrie (anesthésie chez un patient atteint de) --- r_associated #0: 22 --> en:deafness, autosomal recessive 1a
    n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=22
  791. Maladie de Tay-Sachs --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=Maladie de Tay-Sachs | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  792. Marfan (maladie de) --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=Marfan (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  793. acidurie argininosuccinique --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=acidurie argininosuccinique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  794. adipose douloureuse de Dercum --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=adipose douloureuse de Dercum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  795. agnosie des visages --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=agnosie des visages | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  796. alcaptonurie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=alcaptonurie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  797. anasarque f?toplacentaire --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=anasarque f?toplacentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  798. aniridie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=aniridie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  799. argininémie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=argininémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  800. calciphylaxie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=calciphylaxie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  801. choroïdérémie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=choroïdérémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  802. coproporphyrie héréditaire --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=coproporphyrie héréditaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  803. dégénérescence wallerienne --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=dégénérescence wallerienne | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  804. dégénérescence wallérienne --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=dégénérescence wallérienne | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  805. en:Friedreich ataxia --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:Friedreich ataxia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  806. en:alligator skin --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:alligator skin | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  807. en:amyoplasia congenita --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:amyoplasia congenita | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  808. en:congenital porphyria --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:congenital porphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  809. en:noma --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:noma | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  810. en:yellow nail --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=en:yellow nail | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  811. idiosyncrasie au fructose --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=idiosyncrasie au fructose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  812. lichen ruber acuminatus --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=lichen ruber acuminatus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  813. pemphigus bénin des muqueuses --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=pemphigus bénin des muqueuses | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  814. syndrome des ongles jaunes --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=syndrome des ongles jaunes | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  815. xérophtalmie --- r_associated #0: 21 --> en:deafness, autosomal recessive 1a
    n1=xérophtalmie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=21
  816. ARTHROGRYPOSE --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=ARTHROGRYPOSE | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  817. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=dysplasie olfactogénitale de De Morsier | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  818. en:1p36 deletion syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:1p36 deletion syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  819. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  820. en:aagenaes syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:aagenaes syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  821. en:abetalipoproteinemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:abetalipoproteinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  822. en:about half of patients report vestibular symptoms --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:about half of patients report vestibular symptoms | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  823. en:achenbach syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:achenbach syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  824. en:achromatopsia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:achromatopsia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  825. en:acrocephalosyndactyly --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:acrocephalosyndactyly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  826. en:acute intermittent porphyria --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:acute intermittent porphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  827. en:alstrom syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:alstrom syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  828. en:amaurosis fugax --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:amaurosis fugax | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  829. en:andersen syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:andersen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  830. en:antithrombin iii deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:antithrombin iii deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  831. en:aprosencephaly --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:aprosencephaly | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  832. en:bartter syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:bartter syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  833. en:bilateral deafness --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:bilateral deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  834. en:brown-sequard syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:brown-sequard syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  835. en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:camurati-engelmann syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  836. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  837. en:carnosinemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:carnosinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  838. en:cartilage hair hypoplasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cartilage hair hypoplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  839. en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  840. en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  841. en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  842. en:chorea --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:chorea | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  843. en:congenital insensitivity to pain with anhidrosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:congenital insensitivity to pain with anhidrosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  844. en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:congenital myasthenic syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  845. en:cor triatriatum --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cor triatriatum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  846. en:cryopyrin-associated periodic syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cryopyrin-associated periodic syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  847. en:cutis laxa --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cutis laxa | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  848. en:cystathioninuria --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cystathioninuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  849. en:cystinuria --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:cystinuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  850. en:dandy-walker malformation --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:dandy-walker malformation | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  851. en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:de sanctis-cacchione syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  852. en:diffuse cerebral sclerosis of schilder --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:diffuse cerebral sclerosis of schilder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  853. en:diffuse idiopathic skeletal hyperostosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:diffuse idiopathic skeletal hyperostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  854. en:dubowitz syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:dubowitz syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  855. en:dyggve-melchior-clausen syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:dyggve-melchior-clausen syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  856. en:ectromelia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:ectromelia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  857. en:encephalocele --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:encephalocele | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  858. en:epidermolysis bullosa --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:epidermolysis bullosa | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  859. en:erythrokeratodermia variabilis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:erythrokeratodermia variabilis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  860. en:familial juvenile nephronophthisis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:familial juvenile nephronophthisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  861. en:familial mediterranean fever --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:familial mediterranean fever | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  862. en:felty syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:felty syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  863. en:fetal akinesia deformation sequence --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:fetal akinesia deformation sequence | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  864. en:fibromuscular dysplasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:fibromuscular dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  865. en:fraser syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:fraser syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  866. en:fryns syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:fryns syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  867. en:fuchs endothelial dystrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:fuchs endothelial dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  868. en:gastric antral vascular ectasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gastric antral vascular ectasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  869. en:gastroschisis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gastroschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  870. en:genu varum --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:genu varum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  871. en:giant axonal neuropathy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:giant axonal neuropathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  872. en:gjb2, arg143gln --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, arg143gln | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  873. en:gjb2, leu90pro --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gjb2, leu90pro | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  874. en:glycine encephalopathy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:glycine encephalopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  875. en:goodpasture syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:goodpasture syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  876. en:gynatresia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gynatresia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  877. en:gyrate atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:gyrate atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  878. en:hajdu-cheney syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hajdu-cheney syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  879. en:hearing loss --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hearing loss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  880. en:hellp syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hellp syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  881. en:hemochromatosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hemochromatosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  882. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hemophagocytic lymphohistiocytosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  883. en:hemorrhagic fever with renal syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hemorrhagic fever with renal syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  884. en:hepatolenticular degeneration --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hepatolenticular degeneration | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  885. en:high frequency hearing loss --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:high frequency hearing loss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  886. en:homocystinuria --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:homocystinuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  887. en:hyperglycerolemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hyperglycerolemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  888. en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  889. en:hypoalphalipoproteinemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hypoalphalipoproteinemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  890. en:hypokalemic periodic paralysis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hypokalemic periodic paralysis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  891. en:hypophosphatasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:hypophosphatasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  892. en:idiopathic cd4-positive t-lymphocytopenia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:idiopathic cd4-positive t-lymphocytopenia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  893. en:immunoglobulin a deficiency 1 --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:immunoglobulin a deficiency 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  894. en:imperforate vagina --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:imperforate vagina | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  895. en:incontinentia pigmenti --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:incontinentia pigmenti | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  896. en:intestinal atresia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:intestinal atresia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  897. en:jeune syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:jeune syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  898. en:joubert syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:joubert syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  899. en:kartagener syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:kartagener syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  900. en:klippel-feil syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:klippel-feil syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  901. en:klippel-trenaunay-weber syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:klippel-trenaunay-weber syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  902. en:kluver-bucy syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:kluver-bucy syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  903. en:kniest dysplasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:kniest dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  904. en:lafora disease --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:lafora disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  905. en:landau-kleffner syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:landau-kleffner syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  906. en:lateral medullary syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:lateral medullary syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  907. en:leber congenital amaurosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:leber congenital amaurosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  908. en:leber hereditary optic atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:leber hereditary optic atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  909. en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:lecithin acyltransferase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  910. en:lennox-gastaut syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:lennox-gastaut syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  911. en:leptospirosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:leptospirosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  912. en:leukodystrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:leukodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  913. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  914. en:loeys-dietz syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:loeys-dietz syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  915. en:machado-joseph disease --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:machado-joseph disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  916. en:malakoplakia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:malakoplakia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  917. en:malformations of cortical development --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:malformations of cortical development | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  918. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  919. en:mansonelliasis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mansonelliasis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  920. en:mayer-rokitansky-kuster-hauser syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  921. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  922. en:melkersson-rosenthal syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:melkersson-rosenthal syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  923. en:melorheostosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:melorheostosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  924. en:merrf syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:merrf syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  925. en:methylmalonic acidemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:methylmalonic acidemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  926. en:mevalonate kinase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mevalonate kinase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  927. en:migrating partial seizures in infancy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:migrating partial seizures in infancy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  928. en:mixed connective tissue disease --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mixed connective tissue disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  929. en:mmih syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mmih syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  930. en:molybdenum cofactor deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:molybdenum cofactor deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  931. en:monilethrix --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:monilethrix | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  932. en:moyamoya disease --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:moyamoya disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  933. en:muenke syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:muenke syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  934. en:mulibrey nanism --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:mulibrey nanism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  935. en:multiple system atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:multiple system atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  936. en:muscular dystrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:muscular dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  937. en:nadh dehydrogenase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:nadh dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  938. en:nephrogenic fibrosing dermopathy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:nephrogenic fibrosing dermopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  939. en:neuromyelitis optica --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:neuromyelitis optica | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  940. en:noise induced deafness --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:noise induced deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  941. en:ochronosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:ochronosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  942. en:oculocerebrorenal syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:oculocerebrorenal syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  943. en:olivopontocerebellar atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:olivopontocerebellar atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  944. en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:orofaciodigital syndrome type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  945. en:otopalatodigital syndrome type 1 --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:otopalatodigital syndrome type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  946. en:pallister-hall syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pallister-hall syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  947. en:pallister-killian syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pallister-killian syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  948. en:pancreatic lipase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pancreatic lipase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  949. en:pantothenate kinase-associated neurodegeneration --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pantothenate kinase-associated neurodegeneration | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  950. en:pemphigoid gestationis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pemphigoid gestationis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  951. en:peters-plus syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:peters-plus syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  952. en:phosphoenolpyruvate carboxykinase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:phosphoenolpyruvate carboxykinase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  953. en:pinta --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pinta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  954. en:piriformis muscle syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:piriformis muscle syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  955. en:pityriasis lichenoides --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pityriasis lichenoides | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  956. en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:popliteal pterygium syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  957. en:porokeratosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:porokeratosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  958. en:potocki-lupski syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:potocki-lupski syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  959. en:prekallikrein deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:prekallikrein deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  960. en:primary hypertrophic osteoarthropathy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:primary hypertrophic osteoarthropathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  961. en:progressive muscular atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:progressive muscular atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  962. en:proteus syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:proteus syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  963. en:pseudohermaphroditism --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pseudohermaphroditism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  964. en:pseudohypoaldosteronism --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pseudohypoaldosteronism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  965. en:pseudoxanthoma elasticum --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:pseudoxanthoma elasticum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  966. en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  967. en:retinoschisis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:retinoschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  968. en:scimitar syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:scimitar syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  969. en:scleredema adultorum --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:scleredema adultorum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  970. en:seckel syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:seckel syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  971. en:sitosterolemia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:sitosterolemia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  972. en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:smith-lemli-opitz syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  973. en:spasmodic torticollis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:spasmodic torticollis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  974. en:spinal muscular atrophy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:spinal muscular atrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  975. en:spondyloepimetaphyseal dysplasia, sponastrime type --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:spondyloepimetaphyseal dysplasia, sponastrime type | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  976. en:staphylococcal scalded skin syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:staphylococcal scalded skin syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  977. en:status epilepticus --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:status epilepticus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  978. en:stickler syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:stickler syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  979. en:stiff person syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:stiff person syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  980. en:stiff skin syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:stiff skin syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  981. en:sunct syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:sunct syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  982. en:sweet syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:sweet syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  983. en:swyer james syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:swyer james syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  984. en:syringomyelia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:syringomyelia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  985. en:tangier disease --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:tangier disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  986. en:thanatophoric dysplasia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:thanatophoric dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  987. en:thoracic outlet syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:thoracic outlet syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  988. en:tooth and nail syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:tooth and nail syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  989. en:toxic deafness --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:toxic deafness | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  990. en:tracheobronchomalacia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:tracheobronchomalacia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  991. en:transient global amnesia --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:transient global amnesia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  992. en:trichinosis --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:trichinosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  993. en:trichorhinophalangeal syndrome type i --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:trichorhinophalangeal syndrome type i | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  994. en:true hermaphroditism --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:true hermaphroditism | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  995. en:turner syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:turner syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  996. en:uniparental disomy --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:uniparental disomy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  997. en:usher syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:usher syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  998. en:van der woude syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:van der woude syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  999. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  1000. en:wandering spleen --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:wandering spleen | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  1001. en:weill-marchesani syndrome --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=en:weill-marchesani syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  1002. leptospirose --- r_associated #0: 20 --> en:deafness, autosomal recessive 1a
    n1=leptospirose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
  1003. Albert (position d') --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Albert (position d') | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1004. Anomalie d'Ebstein --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Anomalie d'Ebstein | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1005. Arthrogrypose --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Arthrogrypose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1006. Giessen (test de) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Giessen (test de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1007. Intolérance au fructose --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Intolérance au fructose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1008. Kallman --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Kallman | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1009. Maladie de Marfan --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Maladie de Marfan | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1010. Noma --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=Noma | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1011. acidoses lactiques (classification selon Cohen et Woods) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1012. agglutinines froides (neuropathie à) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=agglutinines froides (neuropathie à) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1013. cysticercoïde (larve) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=cysticercoïde (larve) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1014. dysembryome (bénin, malin) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=dysembryome (bénin, malin) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1015. démence (sémiologie) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=démence (sémiologie) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1016. glaucome aigu (crise de) --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=glaucome aigu (crise de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1017. goltz --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=goltz | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1018. hypophosphatasie --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=hypophosphatasie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1019. iceberg (signe de l') --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=iceberg (signe de l') | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1020. maladie à virus de marburg --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=maladie à virus de marburg | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1021. osteopœcilie --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=osteopœcilie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1022. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Kallman-de Morsier | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1023. syndrome de Plummer-VInson --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Plummer-VInson | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1024. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=syndrome de de Morsier-Kallmann | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1025. xérophthalmie --- r_associated #0: 15 --> en:deafness, autosomal recessive 1a
    n1=xérophthalmie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=15
  1026. aprosencéphalie --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=aprosencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1027. dysautonomie familiale --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=dysautonomie familiale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1028. insomnie familiale fatale --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=insomnie familiale fatale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1029. lepréchaunisme --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=lepréchaunisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1030. maladie de Fox-Fordyce --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=maladie de Fox-Fordyce | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1031. maladie de Friedreich --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=maladie de Friedreich | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1032. rétinoschisis --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=rétinoschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1033. syndrome de Gitelman --- r_associated #0: 11 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Gitelman | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=11
  1034. Acromégalie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Acromégalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1035. Agnosie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Agnosie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1036. Albinisme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Albinisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1037. Anencéphalie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Anencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1038. Cataplexie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Cataplexie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1039. Craniosynostose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Craniosynostose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1040. Cysticercose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Cysticercose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1041. Dercum (maladie de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Dercum (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1042. Glycogénose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Glycogénose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1043. HELLP syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=HELLP syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1044. HLP3 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=HLP3 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1045. HPE3 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=HPE3 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1046. HPE4 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=HPE4 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1047. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Haltia-Santavuori (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1048. Hyde (prurigo nodulaire de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Hyde (prurigo nodulaire de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1049. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Insler et Bernstein (score cervical d') | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1050. Levine-Critchley (syndrome de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Levine-Critchley (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1051. Lisfranc (fracture de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Lisfranc (fracture de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1052. Léproserie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Léproserie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1053. Malformation d'Ebstein --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Malformation d'Ebstein | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1054. Marburg (fièvre de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Marburg (fièvre de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1055. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Martin-Bell (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1056. Myosite --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Myosite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1057. Oto-rhino-laryngologiste --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Oto-rhino-laryngologiste | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1058. Otorhinolaryngologiste --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Otorhinolaryngologiste | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1059. PMDS --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=PMDS | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1060. PMI gene --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=PMI gene | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1061. Panum (aire de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Panum (aire de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1062. Peste noire --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Peste noire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1063. Pitt-Rogers-Danks (syndrome de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Pitt-Rogers-Danks (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1064. Progéria --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Progéria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1065. Prosopagnosie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Prosopagnosie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1066. Shy-Drager (syndrome de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Shy-Drager (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1067. Situs inversus --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Situs inversus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1068. Stargardt (maladie de ) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Stargardt (maladie de ) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1069. Stilling-Türk-Duane (syndrome de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Stilling-Türk-Duane (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1070. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1071. Syndrome de Sotos --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Syndrome de Sotos | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1072. Trichothiodystrophie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Trichothiodystrophie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1073. Wegener (granulomatose de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Wegener (granulomatose de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1074. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=Yellen-Gomco (clamp de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1075. a-bêta-lipoprotéinémie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=a-bêta-lipoprotéinémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1076. achondrogénèses --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=achondrogénèses | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1077. achromatopsie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=achromatopsie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1078. alcalose métabolique (classification) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=alcalose métabolique (classification) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1079. angl. XLSA/A --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=angl. XLSA/A | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1080. aniline (intoxication par l') --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=aniline (intoxication par l') | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1081. chondrodysplasie ponctuée --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=chondrodysplasie ponctuée | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1082. coproantigènes (recherche de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=coproantigènes (recherche de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1083. cutis laxa --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=cutis laxa | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1084. diabète bronzé --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=diabète bronzé | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1085. distance interpédiculaire (mesure de la) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=distance interpédiculaire (mesure de la) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1086. dysplasie frontométaphysaire --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=dysplasie frontométaphysaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1087. dysplasie génitale --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=dysplasie génitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1088. dysplasie iridodentaire --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=dysplasie iridodentaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1089. dystrophie musculaire --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=dystrophie musculaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1090. déficit en phosphatases alcalines --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=déficit en phosphatases alcalines | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1091. ectodermitis erosiva pluriorificialis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectodermitis erosiva pluriorificialis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1092. ectodermose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectodermose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1093. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1094. ectoenzyme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectoenzyme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1095. ectomie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectomie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1096. ectomorphie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectomorphie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1097. ectoparasite --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectoparasite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1098. ectoparasitose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectoparasitose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1099. ectopie cardiaque --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectopie cardiaque | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1100. ectopie des procès ciliaires --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectopie des procès ciliaires | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1101. ectopie du cristallin --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ectopie du cristallin | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1102. en:5q microdeletion --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:5q microdeletion | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1103. en:Albert's position --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Albert's position | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1104. en:Albright's hereditary osteodystrophy --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Albright's hereditary osteodystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1105. en:Cogan-Reese syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Cogan-Reese syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1106. en:Crouzon's disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Crouzon's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1107. en:Crouzon?s disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Crouzon?s disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1108. en:FrontoMetaphyseal Dysplasia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:FrontoMetaphyseal Dysplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1109. en:Holt-Oram syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Holt-Oram syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1110. en:Jadassohn-Lewandowsky syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Jadassohn-Lewandowsky syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1111. en:LEOPARD syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:LEOPARD syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1112. en:MELAS syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:MELAS syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1113. en:NHSA III --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:NHSA III | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1114. en:Perthes' disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Perthes' disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1115. en:Riley-Day's syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Riley-Day's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1116. en:Schmorl's jaundice --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Schmorl's jaundice | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1117. en:Schridde's disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Schridde's disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1118. en:Shy-Drager's syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Shy-Drager's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1119. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Smith-Magenis syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1120. en:Sotos's syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Sotos's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1121. en:Stilling-Türk-Duane's syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Stilling-Türk-Duane's syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1122. en:Tay Sachs' disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Tay Sachs' disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1123. en:WBS --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:WBS | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1124. en:Williams' syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Williams' syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1125. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:Williams-Beuren syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1126. en:abdominal wall aplasia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:abdominal wall aplasia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1127. en:acromegalia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:acromegalia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1128. en:acute glaucoma --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:acute glaucoma | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1129. en:adactylia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:adactylia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1130. en:alcaptonuria --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:alcaptonuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1131. en:anacousia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:anacousia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1132. en:anaesthesia for porphyria --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:anaesthesia for porphyria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1133. en:and oligophrenia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:and oligophrenia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1134. en:and photophobia syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:and photophobia syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1135. en:and postaxil polydactylie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:and postaxil polydactylie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1136. en:atresia ani --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:atresia ani | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1137. en:atrichia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:atrichia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1138. en:bilirubin encephalopathy --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:bilirubin encephalopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1139. en:cancrum oris --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:cancrum oris | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1140. en:congenital insensitivity to pain type III --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:congenital insensitivity to pain type III | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1141. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:ectrodactyly and macular dystrophy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1142. en:erythroblastosis fetalis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:erythroblastosis fetalis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1143. en:follicularis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:follicularis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1144. en:glycogenosis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:glycogenosis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1145. en:green monkey virus disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:green monkey virus disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1146. en:hereditary sensory and autonomic neuropathy type III --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:hereditary sensory and autonomic neuropathy type III | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1147. en:homogentisuria --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:homogentisuria | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1148. en:inability to recognize faces --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:inability to recognize faces | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1149. en:infectious gangrene of the mouth --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:infectious gangrene of the mouth | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1150. en:irideremia --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:irideremia | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1151. en:leper house --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:leper house | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1152. en:lughole --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:lughole | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1153. en:minimal pigment type --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:minimal pigment type | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1154. en:nuclear icterus --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:nuclear icterus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1155. en:nuclear jaundice --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:nuclear jaundice | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1156. en:optic neuropathy --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:optic neuropathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1157. en:patterson-kelly syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:patterson-kelly syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1158. en:peripheral neuropathy in cold agglutinin disease --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:peripheral neuropathy in cold agglutinin disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1159. en:schitzel --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:schitzel | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1160. en:secondary degeneration --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:secondary degeneration | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1161. en:sign of the iceberg --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:sign of the iceberg | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1162. en:spastic neurologic disorder --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:spastic neurologic disorder | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1163. en:stress cardiomyopathy --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:stress cardiomyopathy | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1164. en:type 1 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:type 1 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1165. en:type 2 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:type 2 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1166. en:type 3 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:type 3 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1167. en:type 4 --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:type 4 | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1168. en:wallerian degeneraton --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:wallerian degeneraton | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1169. en:xanthine lithiasis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:xanthine lithiasis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1170. en:xanthonychia syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:xanthonychia syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1171. en:xanthonychie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=en:xanthonychie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1172. encéphalocèle --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=encéphalocèle | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1173. fente nasolabiopalatine --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=fente nasolabiopalatine | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1174. gastroschisis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=gastroschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1175. genu varum --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=genu varum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1176. glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=glycogénique (surcharge et infiltration) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1177. holocentromère --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holocentromère | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1178. holocentromérique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holocentromérique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1179. holocrine --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holocrine | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1180. holodiastolique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holodiastolique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1181. holoenzyme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holoenzyme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1182. hologamie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hologamie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1183. hologynique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hologynique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1184. holomérocrine --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holomérocrine | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1185. holophrase --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holophrase | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1186. holoproencéphalie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=holoproencéphalie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1187. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1188. hypohypophysie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hypohypophysie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1189. hypophosphatasies --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hypophosphatasies | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1190. hypostimulinie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hypostimulinie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1191. hémochromatose primitive --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=hémochromatose primitive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1192. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=impédance acoustique (symb. Z) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1193. incontinentia pigmenti --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=incontinentia pigmenti | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1194. laparoschisis --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=laparoschisis | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1195. maladie de Stargardt --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=maladie de Stargardt | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1196. maladie de Tangier --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=maladie de Tangier | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1197. neuroblastome (mise en évidence scintigraphique du) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=neuroblastome (mise en évidence scintigraphique du) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1198. néphritique (syndrome) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=néphritique (syndrome) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1199. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1200. paralysie périodique hypokaliémique familiale (maladie de Westphal) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=paralysie périodique hypokaliémique familiale (maladie de Westphal) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1201. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1202. pinta --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pinta | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1203. pluripotence --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pluripotence | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1204. pluripotent --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pluripotent | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1205. plurisegmentectomie hépatique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=plurisegmentectomie hépatique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1206. pneumallergène --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumallergène | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1207. pneumatisation de l'apophyse unciforme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumatisation de l'apophyse unciforme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1208. pneumatisation du cornet moyen --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumatisation du cornet moyen | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1209. pneumatocèle --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumatocèle | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1210. pneumatose colique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumatose colique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1211. pneumaturie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumaturie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1212. pneumectomie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumectomie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1213. pneumoarthrographie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumoarthrographie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1214. pneumobilie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pneumobilie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1215. profondeur de l'anesthésie (stade de) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=profondeur de l'anesthésie (stade de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1216. prolidase (déficit en) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=prolidase (déficit en) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1217. protéine trifonctionnelle mitochondriale (déficit en) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=protéine trifonctionnelle mitochondriale (déficit en) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1218. pseudo-hypoaldostéronisme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pseudo-hypoaldostéronisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1219. pseudohypoaldostéronisme --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=pseudohypoaldostéronisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1220. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1221. rate aberrante --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=rate aberrante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1222. rate flottante --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=rate flottante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1223. rate vagabonde --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=rate vagabonde | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1224. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=rétinite pigmentaire et retard mental | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1225. seitelberger --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=seitelberger | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1226. sel biliaire --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=sel biliaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1227. sirtuine --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=sirtuine | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1228. sisi-test --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=sisi-test | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1229. sismothérapie --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=sismothérapie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1230. situs inversus viscerum --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=situs inversus viscerum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1231. situs mutatus --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=situs mutatus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1232. souche de référence --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=souche de référence | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1233. souche transduite --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=souche transduite | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1234. splénoptose --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=splénoptose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1235. stiff skin syndrome --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=stiff skin syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1236. surdité --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=surdité | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1237. syndrome de Feingold --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Feingold | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1238. syndrome de Korsakoff --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Korsakoff | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1239. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1240. syndrome de Rathbun --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Rathbun | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1241. syndrome de Rokitansky --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Rokitansky | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1242. syndrome de Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Rokitansky-Küster-Hauser | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1243. syndrome de de Morsier --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome de de Morsier | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1244. syndrome des pouces en adduction-arthrogrypose (type Dundar) --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=syndrome des pouces en adduction-arthrogrypose (type Dundar) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1245. sélacien venimeux --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=sélacien venimeux | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1246. état de mal épileptique --- r_associated #0: 10 --> en:deafness, autosomal recessive 1a
    n1=état de mal épileptique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=10
  1247. dysencéphalie splanchnokystique --- r_associated #0: 6 --> en:deafness, autosomal recessive 1a
    n1=dysencéphalie splanchnokystique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=6
  1248. Acinetobacter --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Acinetobacter | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1249. Anasarque --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Anasarque | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1250. Hypopituitarisme --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Hypopituitarisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1251. Neurocysticercose --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Neurocysticercose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1252. Neuropathie optique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Neuropathie optique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1253. Onsager (relation d') --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Onsager (relation d') | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1254. Perthes (maladie de) --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Perthes (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1255. Peste Noire --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Peste Noire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1256. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Tay-Sachs (maladie de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1257. Williams (syndrome de) --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=Williams (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1258. abêtalipoprotéinémie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=abêtalipoprotéinémie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1259. acidurie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acidurie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1260. acidurie 3-hydroxy-3-méthyl-glutarique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1261. acidurie 3-méthylglutaconique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acidurie 3-méthylglutaconique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1262. acidurie 4-hydroxybutyrique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acidurie 4-hydroxybutyrique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1263. acidurie paradoxale --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acidurie paradoxale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1264. acineux --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acineux | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1265. acini --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acini | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1266. acinus --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acinus | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1267. acinus hépatique de Rappaport --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=acinus hépatique de Rappaport | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1268. agglutinines irrégulières --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agglutinines irrégulières | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1269. agglutinogène --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agglutinogène | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1270. agitation postopératoire --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agitation postopératoire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1271. aglossie et adactylie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=aglossie et adactylie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1272. aglycone --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=aglycone | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1273. agnosie chromatique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agnosie chromatique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1274. agnosie d'extensité --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agnosie d'extensité | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1275. agnosie d'intensité --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agnosie d'intensité | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1276. agnosie des couleurs --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=agnosie des couleurs | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1277. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1278. albinisme avec surdité --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=albinisme avec surdité | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1279. amnésie globale transitoire --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=amnésie globale transitoire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1280. disomie uniparentale --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=disomie uniparentale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1281. dysembryome cutané --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysembryome cutané | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1282. dysembryome de l'ovaire --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysembryome de l'ovaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1283. dysembryome testiculaire --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysembryome testiculaire | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1284. dysembryoplasie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysembryoplasie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1285. dysembryoplasie neuro-épithéliale --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysembryoplasie neuro-épithéliale | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1286. dysenterie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysenterie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1287. dysenterie amibienne --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysenterie amibienne | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1288. dysentériforme --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysentériforme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1289. dysentérique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysentérique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1290. dysérythropoïèse --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=dysérythropoïèse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1291. démence d'Alzheimer --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=démence d'Alzheimer | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1292. en:Sachs' disease --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=en:Sachs' disease | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1293. en:Seckel syndrome --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=en:Seckel syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1294. fibrose systémique néphrogénique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=fibrose systémique néphrogénique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1295. hémochromatose --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=hémochromatose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1296. ichtyophtalmie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=ichtyophtalmie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1297. ichtyosarcotoxisme --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=ichtyosarcotoxisme | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1298. insectes (allergie aux) --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=insectes (allergie aux) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1299. myopathie primitive progressive --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=myopathie primitive progressive | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1300. mésentérite rétractile --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=mésentérite rétractile | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1301. mésentérite sclérosante --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=mésentérite sclérosante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1302. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1303. onychodysplasie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onychodysplasie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1304. onychogryphose --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onychogryphose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1305. onycholyse --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onycholyse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1306. onycholyse candidosique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onycholyse candidosique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1307. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onycholyse semi-lunaire partielle | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1308. onychomadèse --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onychomadèse | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1309. onychomatricome --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=onychomatricome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1310. osteopoecilie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=osteopoecilie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1311. paragnathe --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=paragnathe | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1312. pemphigoïde muqueux bénin --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=pemphigoïde muqueux bénin | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1313. porphyrie aigüe intermittente --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=porphyrie aigüe intermittente | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1314. porphyrie cutanée --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=porphyrie cutanée | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1315. porphyrie de Doss --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=porphyrie de Doss | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1316. ptose splénique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=ptose splénique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1317. rate ectopique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=rate ectopique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1318. rate errante --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=rate errante | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1319. syndrome de Stickler --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Stickler | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1320. syndrome de Waterhouse-Friderichsen --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=syndrome de Waterhouse-Friderichsen | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1321. syndrome olfacto-génital --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=syndrome olfacto-génital | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1322. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthoastrocytome pléomorphe | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1323. xanthochromie --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthochromie | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1324. xanthochromie caroténique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthochromie caroténique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1325. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthoerythrodermia perstans | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1326. xanthogranulome juvénile --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthogranulome juvénile | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1327. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthogranulome nécrobiotique | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1328. xanthogranulome palpébral --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthogranulome palpébral | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1329. xanthohistiocytome --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthohistiocytome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1330. xanthoma disseminatum --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthoma disseminatum | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1331. xanthomatose --- r_associated #0: 5 --> en:deafness, autosomal recessive 1a
    n1=xanthomatose | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=5
  1332. escalope --- r_associated #0: -20 --> en:deafness, autosomal recessive 1a
    n1=escalope | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=-20
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