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'en:childhood hypophosphatasia (disorder)'
(id=6818827 ; fe=en:childhood hypophosphatasia (disorder) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=29656.54998779297 creation date=2017-06-25 touchdate=2025-08-21 11:21:17.000)
≈ 592 relations sortantes

  1. en:childhood hypophosphatasia (disorder) -- r_associated #0: 43 / 1 -> en:hereditary orotic aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=43
  2. en:childhood hypophosphatasia (disorder) -- r_associated #0: 43 / 1 -> en:microcephaly, amish type (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=43
  3. en:childhood hypophosphatasia (disorder) -- r_associated #0: 43 / 1 -> en:pancreatic alpha-amylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pancreatic alpha-amylase deficiency | rel=r_associated | relid=0 | w=43
  4. en:childhood hypophosphatasia (disorder) -- r_associated #0: 43 / 1 -> en:sonoda syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=43
  5. en:childhood hypophosphatasia (disorder) -- r_associated #0: 42 / 0.977 -> en:alpl, arg119his
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, arg119his | rel=r_associated | relid=0 | w=42
  6. en:childhood hypophosphatasia (disorder) -- r_associated #0: 42 / 0.977 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=42
  7. en:childhood hypophosphatasia (disorder) -- r_associated #0: 42 / 0.977 -> en:marles greenberg persaud syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=42
  8. en:childhood hypophosphatasia (disorder) -- r_associated #0: 42 / 0.977 -> en:transcobalamin ii deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=42
  9. en:childhood hypophosphatasia (disorder) -- r_associated #0: 41 / 0.953 -> en:adult hypophosphatasia (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:adult hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  10. en:childhood hypophosphatasia (disorder) -- r_associated #0: 41 / 0.953 -> en:pseudotrisomy 13 syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  11. en:childhood hypophosphatasia (disorder) -- r_associated #0: 41 / 0.953 -> en:waddling gait
    n1=en:childhood hypophosphatasia (disorder) | n2=en:waddling gait | rel=r_associated | relid=0 | w=41
  12. en:childhood hypophosphatasia (disorder) -- r_associated #0: 40 / 0.93 -> en:pelizaeus merzbacher like disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=40
  13. en:childhood hypophosphatasia (disorder) -- r_associated #0: 40 / 0.93 -> en:ugt1a1*28 polymorphism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ugt1a1*28 polymorphism | rel=r_associated | relid=0 | w=40
  14. en:childhood hypophosphatasia (disorder) -- r_associated #0: 40 / 0.93 -> en:xanthinuria, type i
    n1=en:childhood hypophosphatasia (disorder) | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=40
  15. en:childhood hypophosphatasia (disorder) -- r_associated #0: 39 / 0.907 -> en:3-methylglutaconic aciduria type 3
    n1=en:childhood hypophosphatasia (disorder) | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=39
  16. en:childhood hypophosphatasia (disorder) -- r_associated #0: 39 / 0.907 -> en:autosomal recessive ichthyosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=39
  17. en:childhood hypophosphatasia (disorder) -- r_associated #0: 39 / 0.907 -> en:homocarnosinosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:homocarnosinosis | rel=r_associated | relid=0 | w=39
  18. en:childhood hypophosphatasia (disorder) -- r_associated #0: 39 / 0.907 -> en:skin dimple over apex of long bone angulation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:skin dimple over apex of long bone angulation | rel=r_associated | relid=0 | w=39
  19. en:childhood hypophosphatasia (disorder) -- r_associated #0: 39 / 0.907 -> en:verloes bourguignon syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=39
  20. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:atrophoderma vermiculatum
    n1=en:childhood hypophosphatasia (disorder) | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=38
  21. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:basal ganglia disease, biotin-responsive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=38
  22. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=38
  23. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:cystathionine beta-synthase deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=38
  24. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=38
  25. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:gurrieri sammito bellussi syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=38
  26. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:hmg-coa lyase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=38
  27. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:hyperprolinemia type 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=38
  28. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:childhood hypophosphatasia (disorder) | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=38
  29. en:childhood hypophosphatasia (disorder) -- r_associated #0: 38 / 0.884 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=38
  30. en:childhood hypophosphatasia (disorder) -- r_associated #0: 37 / 0.86 -> en:pseudocholinesterase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=37
  31. en:childhood hypophosphatasia (disorder) -- r_associated #0: 36 / 0.837 -> en:acrodermatitis enteropathica
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=36
  32. en:childhood hypophosphatasia (disorder) -- r_associated #0: 36 / 0.837 -> en:classical phenylketonuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=36
  33. en:childhood hypophosphatasia (disorder) -- r_associated #0: 36 / 0.837 -> en:congenital adrenal hyperplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=36
  34. en:childhood hypophosphatasia (disorder) -- r_associated #0: 36 / 0.837 -> en:disorder due to n-acetyltransferase enzyme variant
    n1=en:childhood hypophosphatasia (disorder) | n2=en:disorder due to n-acetyltransferase enzyme variant | rel=r_associated | relid=0 | w=36
  35. en:childhood hypophosphatasia (disorder) -- r_associated #0: 36 / 0.837 -> en:maple syrup urine disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=36
  36. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:al awadi syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=35
  37. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:alpha-1 antitrypsin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=35
  38. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=35
  39. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=35
  40. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal recessive asexual dwarfism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=35
  41. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=35
  42. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=35
  43. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=35
  44. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:charcot-marie-tooth disease type 4
    n1=en:childhood hypophosphatasia (disorder) | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=35
  45. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:childhood
    n1=en:childhood hypophosphatasia (disorder) | n2=en:childhood | rel=r_associated | relid=0 | w=35
  46. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:citrullinemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:citrullinemia | rel=r_associated | relid=0 | w=35
  47. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:combined malonic and methylmalonic aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=35
  48. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=35
  49. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:cytochrome-c oxidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=35
  50. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:ear, patella, short stature syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=35
  51. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=35
  52. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:elevated plasma and urine inorganic pyrophosphate (ppi)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:elevated plasma and urine inorganic pyrophosphate (ppi) | rel=r_associated | relid=0 | w=35
  53. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=35
  54. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:genu varum
    n1=en:childhood hypophosphatasia (disorder) | n2=en:genu varum | rel=r_associated | relid=0 | w=35
  55. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:giacci familial neurogenic acroosteolysis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=35
  56. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:hereditary fructose intolerance
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=35
  57. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:hyperphosphatasia with mental retardation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=35
  58. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:hypokalemia, familial
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=35
  59. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=35
  60. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:joubert syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=35
  61. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:lactose intolerance, adult type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lactose intolerance, adult type | rel=r_associated | relid=0 | w=35
  62. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=35
  63. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:leukotriene c4 synthase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=35
  64. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=35
  65. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=35
  66. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:multiple sulfatase deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=35
  67. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:myopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:myopathy | rel=r_associated | relid=0 | w=35
  68. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:naxos disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:naxos disease | rel=r_associated | relid=0 | w=35
  69. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:pentosuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pentosuria | rel=r_associated | relid=0 | w=35
  70. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=35
  71. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:pontocerebellar hypoplasia type 2
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=35
  72. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:primary hyperoxaluria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=35
  73. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:sitosterolemia with xanthomatosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=35
  74. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:specific enzyme deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:specific enzyme deficiency | rel=r_associated | relid=0 | w=35
  75. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=35
  76. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:childhood hypophosphatasia (disorder) | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=35
  77. en:childhood hypophosphatasia (disorder) -- r_associated #0: 35 / 0.814 -> en:valinemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:valinemia | rel=r_associated | relid=0 | w=35
  78. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:3-methylglutaconic aciduria type iv
    n1=en:childhood hypophosphatasia (disorder) | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=34
  79. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=34
  80. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:ataxia telangiectasia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=34
  81. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:behr syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:behr syndrome | rel=r_associated | relid=0 | w=34
  82. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:beta-aminoisobutyricaciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=34
  83. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:chylomicron retention disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  84. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:citrin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=34
  85. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:cohen syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=34
  86. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:congenital leptin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=34
  87. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:congenital sucrase-isomaltase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=34
  88. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:deficiency of glucosyltransferase 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=34
  89. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:donnai-barrow syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=34
  90. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=34
  91. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:glutamate formiminotransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=34
  92. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=34
  93. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:glycogen storage disease type i
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=34
  94. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:hereditary factor xii deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=34
  95. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:i-cell disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:i-cell disease | rel=r_associated | relid=0 | w=34
  96. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:infantile globoid cell leukodystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=34
  97. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:laron syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:laron syndrome | rel=r_associated | relid=0 | w=34
  98. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:laurence-moon syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=34
  99. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:lethal congenital contracture syndrome type 3
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=34
  100. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:low alkaline phosphatase
    n1=en:childhood hypophosphatasia (disorder) | n2=en:low alkaline phosphatase | rel=r_associated | relid=0 | w=34
  101. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:macdermot winter syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=34
  102. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:macular corneal dystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=34
  103. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:majeed syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=34
  104. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:microcephaly-capillary malformation syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  105. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:mucopolysaccharidosis type i
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=34
  106. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:muscle l-lactate dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  107. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:myopathy with exercise intolerance, swedish type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=34
  108. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=34
  109. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=34
  110. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:north american indian childhood cirrhosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=34
  111. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:porphobilinogen synthase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=34
  112. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:prolonged electroretinal response suppression
    n1=en:childhood hypophosphatasia (disorder) | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=34
  113. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=34
  114. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:richards-rundle syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=34
  115. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=34
  116. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:tungland bellman syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=34
  117. en:childhood hypophosphatasia (disorder) -- r_associated #0: 34 / 0.791 -> en:urocanase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=34
  118. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=32
  119. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:adrenal gland hyperplasia ii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=32
  120. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:alpha, alpha-trehalase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=32
  121. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:alpl, ala99thr
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, ala99thr | rel=r_associated | relid=0 | w=32
  122. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:alpl, gly232val
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, gly232val | rel=r_associated | relid=0 | w=32
  123. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:aminoacylase 1 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=32
  124. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:argininemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:argininemia | rel=r_associated | relid=0 | w=32
  125. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:ataxia with vitamin e deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=32
  126. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:autosomal recessive primary microcephaly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=32
  127. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:autosomal recessive sideroblastic anemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=32
  128. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:baller-gerold syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=32
  129. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:becker generalized myotonia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=32
  130. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=32
  131. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:cerebrotendinous xanthomatosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=32
  132. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=32
  133. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:corpus callosum agenesis neuronopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=32
  134. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:craniosynostosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=32
  135. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:cryptophthalmos syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=32
  136. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:deficiency of fructokinase
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=32
  137. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  138. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:dubin-johnson syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=32
  139. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=32
  140. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:frontal bossing
    n1=en:childhood hypophosphatasia (disorder) | n2=en:frontal bossing | rel=r_associated | relid=0 | w=32
  141. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=32
  142. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=32
  143. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=32
  144. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:histidinemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:histidinemia | rel=r_associated | relid=0 | w=32
  145. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=32
  146. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:hypospadias-mental retardation syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=32
  147. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:lipoprotein glomerulopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=32
  148. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=32
  149. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=32
  150. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:muscle d-lactate dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:muscle d-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  151. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=32
  152. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:neuroacanthocytosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=32
  153. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:neutral lipid storage disease with myopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=32
  154. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:niemann-pick disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=32
  155. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:otoonychoperoneal syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=32
  156. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=32
  157. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:presentation after 6 months
    n1=en:childhood hypophosphatasia (disorder) | n2=en:presentation after 6 months | rel=r_associated | relid=0 | w=32
  158. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:retinitis punctata albescens (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=32
  159. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:rna polymerase iii-related leukodystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=32
  160. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:sarcosinemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=32
  161. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:severe early childhood onset retinal dystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=32
  162. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=32
  163. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:tay-sachs disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=32
  164. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:trichohepatoenteric syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=32
  165. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:type ii acrocephalopolysyndactyly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=32
  166. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> en:tyrosinemia, type iii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=32
  167. en:childhood hypophosphatasia (disorder) -- r_associated #0: 32 / 0.744 -> hypophosphatasie de l'enfant
    n1=en:childhood hypophosphatasia (disorder) | n2=hypophosphatasie de l'enfant | rel=r_associated | relid=0 | w=32
  168. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:acid phosphatase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=31
  169. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:acrocallosal syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=31
  170. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=31
  171. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:alkaptonuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=31
  172. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:alpl, ala176thr
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, ala176thr | rel=r_associated | relid=0 | w=31
  173. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:alpl, arg272cys
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, arg272cys | rel=r_associated | relid=0 | w=31
  174. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:alpl, gly145val
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, gly145val | rel=r_associated | relid=0 | w=31
  175. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:aminomethyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=31
  176. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:ateliotic dwarfism without insulinopenia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=31
  177. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=31
  178. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:autosomal recessive inheritance
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=31
  179. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=31
  180. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:bothnia retinal dystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=31
  181. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:brown-vialetto-van laere syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=31
  182. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:circulating enzyme deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:circulating enzyme deficiency | rel=r_associated | relid=0 | w=31
  183. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=31
  184. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=31
  185. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=31
  186. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:hereditary factor x deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=31
  187. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31
  188. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=31
  189. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:jankovic rivera syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=31
  190. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:kaufman-mckusick syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=31
  191. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:knobloch syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=31
  192. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:lethal congenital contracture syndrome 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=31
  193. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=31
  194. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=31
  195. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:northern epilepsy syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=31
  196. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:oculocutaneous albinism type 4
    n1=en:childhood hypophosphatasia (disorder) | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=31
  197. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:orotic aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=31
  198. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:propionic acidemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=31
  199. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=31
  200. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:seizure
    n1=en:childhood hypophosphatasia (disorder) | n2=en:seizure | rel=r_associated | relid=0 | w=31
  201. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:tetra-amelia autosomal recessive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=31
  202. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=31
  203. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:walker-warburg syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=31
  204. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:walking delay
    n1=en:childhood hypophosphatasia (disorder) | n2=en:walking delay | rel=r_associated | relid=0 | w=31
  205. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> en:wolman disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:wolman disease | rel=r_associated | relid=0 | w=31
  206. en:childhood hypophosphatasia (disorder) -- r_associated #0: 31 / 0.721 -> hypophosphatasie, forme juvénile
    n1=en:childhood hypophosphatasia (disorder) | n2=hypophosphatasie, forme juvénile | rel=r_associated | relid=0 | w=31
  207. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:2-hydroxyglutaric aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=30
  208. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:3-methylglutaconic aciduria type 5
    n1=en:childhood hypophosphatasia (disorder) | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=30
  209. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:acyl-coa dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=30
  210. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:aldosterone synthase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:aldosterone synthase deficiency | rel=r_associated | relid=0 | w=30
  211. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:allanson pantzar mcleod syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=30
  212. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:alpha-fetoprotein deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=30
  213. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:arakawa syndrome ii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=30
  214. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:argininosuccinic aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=30
  215. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:arterial tortuosity syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=30
  216. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:brachydactyly syndrome type b
    n1=en:childhood hypophosphatasia (disorder) | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=30
  217. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:brody myopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:brody myopathy | rel=r_associated | relid=0 | w=30
  218. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=30
  219. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:chitty hall baraitser syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=30
  220. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:congenital disorder of glycosylation type ia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=30
  221. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=30
  222. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:deficiency in enzyme complexes of mitochondrial respiratory chain
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deficiency in enzyme complexes of mitochondrial respiratory chain | rel=r_associated | relid=0 | w=30
  223. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:desmosterolosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=30
  224. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=30
  225. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=30
  226. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:enterokinase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=30
  227. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30
  228. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=30
  229. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=30
  230. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:geroderma osteodysplastica
    n1=en:childhood hypophosphatasia (disorder) | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=30
  231. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:glutathione synthetase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=30
  232. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=30
  233. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:hydroxykynureninuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hydroxykynureninuria | rel=r_associated | relid=0 | w=30
  234. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:hyperprolinemia type 2
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=30
  235. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:hypophosphatasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=30
  236. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=30
  237. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:jervell and lange nielsen syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=30
  238. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:kuskokwim disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=30
  239. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:lactase deficiency, congenital
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=30
  240. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:lipoid congenital adrenal hyperplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lipoid congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=30
  241. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:microcephalic primordial dwarfism toriello type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=30
  242. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:morquio syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=30
  243. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:nonaka myopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=30
  244. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:pancreatic colipase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pancreatic colipase deficiency | rel=r_associated | relid=0 | w=30
  245. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:papillon-lefevre syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=30
  246. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:persistent mullerian duct syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=30
  247. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:phosphate diabetes
    n1=en:childhood hypophosphatasia (disorder) | n2=en:phosphate diabetes | rel=r_associated | relid=0 | w=30
  248. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:premature deciduous tooth loss (less than five years of age)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:premature deciduous tooth loss (less than five years of age) | rel=r_associated | relid=0 | w=30
  249. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:prolidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=30
  250. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:rachitic rosary
    n1=en:childhood hypophosphatasia (disorder) | n2=en:rachitic rosary | rel=r_associated | relid=0 | w=30
  251. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:sanfilippo syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=30
  252. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:sly syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sly syndrome | rel=r_associated | relid=0 | w=30
  253. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=30
  254. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia with epilepsy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=30
  255. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:spondyloenchondrodysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=30
  256. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> en:uv-sensitive syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=30
  257. en:childhood hypophosphatasia (disorder) -- r_associated #0: 30 / 0.698 -> syndrome de Walker-Warburg
    n1=en:childhood hypophosphatasia (disorder) | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=30
  258. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:5-oxoprolinase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=29
  259. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:bowen-conradi syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=29
  260. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:congenital
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital | rel=r_associated | relid=0 | w=29
  261. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:congenital pancreatic enterokinase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=29
  262. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:factor v and factor viii, combined deficiency of
    n1=en:childhood hypophosphatasia (disorder) | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=29
  263. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=29
  264. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:familial renal iminoglycinuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=29
  265. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=29
  266. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:hnsha due to aldolase a deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=29
  267. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:hyperandrogenism due to non-classic 21-hydroxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=29
  268. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:hypomagnesemia 1, intestinal
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=29
  269. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:isolated hyperchlorhidrosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=29
  270. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:isolated hypoplasia of the right ventricle
    n1=en:childhood hypophosphatasia (disorder) | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=29
  271. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:lecithin acyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=29
  272. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:methionine adenosyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=29
  273. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:microcephaly cervical spine fusion anomalies
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=29
  274. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=29
  275. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=29
  276. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:morm syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:morm syndrome | rel=r_associated | relid=0 | w=29
  277. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:childhood hypophosphatasia (disorder) | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=29
  278. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:n-acetylglutamate synthase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=29
  279. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:nathalie syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=29
  280. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:peters-plus syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=29
  281. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=29
  282. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=29
  283. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:short stature
    n1=en:childhood hypophosphatasia (disorder) | n2=en:short stature | rel=r_associated | relid=0 | w=29
  284. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=29
  285. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=29
  286. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=29
  287. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:tyrosinemia type ii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=29
  288. en:childhood hypophosphatasia (disorder) -- r_associated #0: 29 / 0.674 -> en:xeroderma pigmentosum
    n1=en:childhood hypophosphatasia (disorder) | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=29
  289. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:17 alpha-hydroxyprogesterone aldolase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:17 alpha-hydroxyprogesterone aldolase deficiency | rel=r_associated | relid=0 | w=28
  290. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:21-hydroxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=28
  291. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:acquired lactase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acquired lactase deficiency | rel=r_associated | relid=0 | w=28
  292. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=28
  293. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:childhood hypophosphatasia (disorder) | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=28
  294. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:childhood hypophosphatasia (disorder) | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=28
  295. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=28
  296. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal recessive scid
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=28
  297. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:bardet-biedl syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=28
  298. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:biotinidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=28
  299. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:crigler-najjar syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=28
  300. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:cystinosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cystinosis | rel=r_associated | relid=0 | w=28
  301. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:deafness, progressive, with stapes fixation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=28
  302. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:dihydropyrimidinase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dihydropyrimidinase deficiency | rel=r_associated | relid=0 | w=28
  303. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | rel=r_associated | relid=0 | w=28
  304. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:ehlers-danlos syndrome, type vi
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=28
  305. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:childhood hypophosphatasia (disorder) | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=28
  306. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:exophthalmos
    n1=en:childhood hypophosphatasia (disorder) | n2=en:exophthalmos | rel=r_associated | relid=0 | w=28
  307. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:familial hypoaldosteronism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=28
  308. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:ferrochelatase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ferrochelatase deficiency | rel=r_associated | relid=0 | w=28
  309. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:fronto-facio-nasal dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=28
  310. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:gamma-glutamyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=28
  311. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:glutamate-cysteine ligase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=28
  312. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:gracile syndrome (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=28
  313. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:hereditary factor xi deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=28
  314. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:hereditary xanthinuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary xanthinuria | rel=r_associated | relid=0 | w=28
  315. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:hnsha due to glutathione reductase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=28
  316. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=28
  317. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:infantile hypophosphatasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=28
  318. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:isaacs syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=28
  319. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=28
  320. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:mannosidosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mannosidosis | rel=r_associated | relid=0 | w=28
  321. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:maroteaux-lamy syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=28
  322. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:childhood hypophosphatasia (disorder) | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=28
  323. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=28
  324. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=28
  325. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=28
  326. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:muscle amp deaminase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=28
  327. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:peeling skin syndrome, acral type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=28
  328. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=28
  329. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:presentey anomaly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=28
  330. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=28
  331. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:pyruvate carboxylase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=28
  332. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:rapadilino syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=28
  333. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:reardon hall slaney syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=28
  334. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=28
  335. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:smith-mccort dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=28
  336. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=28
  337. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:thyroid dyshormonogenesis 4
    n1=en:childhood hypophosphatasia (disorder) | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=28
  338. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:warsaw breakage syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=28
  339. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:werdnig-hoffmann disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=28
  340. en:childhood hypophosphatasia (disorder) -- r_associated #0: 28 / 0.651 -> en:zellweger syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=28
  341. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:alpl, asp277ala
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alpl, asp277ala | rel=r_associated | relid=0 | w=27
  342. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=27
  343. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:autosomal recessive ocular albinism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=27
  344. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:behrens baumann dust syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=27
  345. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:caries
    n1=en:childhood hypophosphatasia (disorder) | n2=en:caries | rel=r_associated | relid=0 | w=27
  346. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) | rel=r_associated | relid=0 | w=27
  347. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=27
  348. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:childhood hypophosphatasia (disorder) | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=27
  349. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:congenital disorder of glycosylation type ig
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=27
  350. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:congenital transferrin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=27
  351. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:crisponi syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=27
  352. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:cutis laxa, autosomal recessive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=27
  353. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:deficiency of steryl-sulfatase
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deficiency of steryl-sulfatase | rel=r_associated | relid=0 | w=27
  354. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:dicarboxylicaminoaciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=27
  355. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:familial acantholysis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=27
  356. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:fucosidosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fucosidosis | rel=r_associated | relid=0 | w=27
  357. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:hepatolenticular degeneration
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=27
  358. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=27
  359. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=27
  360. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:increased aromatase activity
    n1=en:childhood hypophosphatasia (disorder) | n2=en:increased aromatase activity | rel=r_associated | relid=0 | w=27
  361. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:isovaleric acidemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=27
  362. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:lethal congenital contracture syndrome 2
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=27
  363. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=27
  364. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:lysosomal storage disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=27
  365. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=27
  366. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:neuraminidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=27
  367. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:periodontitis co-occurrent with hypophosphatasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:periodontitis co-occurrent with hypophosphatasia | rel=r_associated | relid=0 | w=27
  368. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:pyle metaphyseal dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=27
  369. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:saito kuba tsuruta syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=27
  370. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=27
  371. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:spondylo-ocular syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=27
  372. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=27
  373. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> en:waardenburg anophthalmia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=27
  374. en:childhood hypophosphatasia (disorder) -- r_associated #0: 27 / 0.628 -> hypophosphatasie juvénile
    n1=en:childhood hypophosphatasia (disorder) | n2=hypophosphatasie juvénile | rel=r_associated | relid=0 | w=27
  375. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:17-beta-hydroxysteroid dehydrogenase 3 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | rel=r_associated | relid=0 | w=26
  376. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:3-methylglutaconic aciduria type 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=26
  377. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=26
  378. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:albinotic fundus
    n1=en:childhood hypophosphatasia (disorder) | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=26
  379. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:allgrove syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=26
  380. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:alstrom syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=26
  381. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:childhood hypophosphatasia (disorder) | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=26
  382. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=26
  383. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:aspartylglycosaminuria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=26
  384. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=26
  385. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:carnitine palmitoyltransferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:carnitine palmitoyltransferase deficiency | rel=r_associated | relid=0 | w=26
  386. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:cerebellar ataxia, cayman type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=26
  387. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:characteristic metaphyseal radiolucency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:characteristic metaphyseal radiolucency | rel=r_associated | relid=0 | w=26
  388. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:chondrodysplasia punctata syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=26
  389. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:congenital bowing of long bone
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=26
  390. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:congenital disorder of glycosylation type ic
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=26
  391. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:congenital dyserythropoietic anemia, type i
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=26
  392. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=26
  393. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:craniodiaphyseal dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=26
  394. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:deafness, sensorineural, and male infertility
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=26
  395. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:disorder due to cytochrome p450 enzyme variant
    n1=en:childhood hypophosphatasia (disorder) | n2=en:disorder due to cytochrome p450 enzyme variant | rel=r_associated | relid=0 | w=26
  396. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:ethanolaminosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=26
  397. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:fryns macrocephaly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=26
  398. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:glutathione s-transferase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glutathione s-transferase deficiency | rel=r_associated | relid=0 | w=26
  399. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:glycogen storage disease type x
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=26
  400. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=26
  401. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:hyperimmunoglobulin e syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=26
  402. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:hypomyelination and congenital cataract
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=26
  403. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:hypophosphatasia, infantile, glu174lys (allelic variant)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypophosphatasia, infantile, glu174lys (allelic variant) | rel=r_associated | relid=0 | w=26
  404. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:intestinal disaccharidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:intestinal disaccharidase deficiency | rel=r_associated | relid=0 | w=26
  405. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:intestinal epithelial dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=26
  406. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:long narrow head
    n1=en:childhood hypophosphatasia (disorder) | n2=en:long narrow head | rel=r_associated | relid=0 | w=26
  407. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:neonatal progeroid syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=26
  408. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:netherton syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=26
  409. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:odontohypophosphatasia (disorder)
    n1=en:childhood hypophosphatasia (disorder) | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  410. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:ornithine carbamoyltransferase deficiency disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=26
  411. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:phenylketonuria ii
    n1=en:childhood hypophosphatasia (disorder) | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=26
  412. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:phosphorus metabolic disorder
    n1=en:childhood hypophosphatasia (disorder) | n2=en:phosphorus metabolic disorder | rel=r_associated | relid=0 | w=26
  413. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:rachitic skeletal changes
    n1=en:childhood hypophosphatasia (disorder) | n2=en:rachitic skeletal changes | rel=r_associated | relid=0 | w=26
  414. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=26
  415. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=26
  416. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:sulfite oxidase deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=26
  417. en:childhood hypophosphatasia (disorder) -- r_associated #0: 26 / 0.605 -> en:thomas syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=26
  418. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:childhood hypophosphatasia (disorder) | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  419. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> acrodermatitis enteropathica
    n1=en:childhood hypophosphatasia (disorder) | n2=acrodermatitis enteropathica | rel=r_associated | relid=0 | w=20
  420. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> bébé bronzé (syndrome du)
    n1=en:childhood hypophosphatasia (disorder) | n2=bébé bronzé (syndrome du) | rel=r_associated | relid=0 | w=20
  421. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Bec de lièvre
    n1=en:childhood hypophosphatasia (disorder) | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
  422. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> bec de lièvre
    n1=en:childhood hypophosphatasia (disorder) | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
  423. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> carie dentaire
    n1=en:childhood hypophosphatasia (disorder) | n2=carie dentaire | rel=r_associated | relid=0 | w=20
  424. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Carie dentaire
    n1=en:childhood hypophosphatasia (disorder) | n2=Carie dentaire | rel=r_associated | relid=0 | w=20
  425. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> caries
    n1=en:childhood hypophosphatasia (disorder) | n2=caries | rel=r_associated | relid=0 | w=20
  426. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:childhood hypophosphatasia (disorder) | n2=congénital | rel=r_associated | relid=0 | w=20
  427. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:childhood hypophosphatasia (disorder) | n2=congenital | rel=r_associated | relid=0 | w=20
  428. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:childhood hypophosphatasia (disorder) | n2=congénitale | rel=r_associated | relid=0 | w=20
  429. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> crânio-sténose
    n1=en:childhood hypophosphatasia (disorder) | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  430. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> craniosténose
    n1=en:childhood hypophosphatasia (disorder) | n2=craniosténose | rel=r_associated | relid=0 | w=20
  431. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> crâniosténose
    n1=en:childhood hypophosphatasia (disorder) | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  432. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> craniosynostose
    n1=en:childhood hypophosphatasia (disorder) | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  433. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> crâniosynostose
    n1=en:childhood hypophosphatasia (disorder) | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  434. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit congénital en mégacaryocytes
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20
  435. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  436. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  437. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  438. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en neuraminidase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20
  439. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  440. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  441. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:childhood hypophosphatasia (disorder) | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  442. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> diabète phosphaté familial chronique
    n1=en:childhood hypophosphatasia (disorder) | n2=diabète phosphaté familial chronique | rel=r_associated | relid=0 | w=20
  443. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire
    n1=en:childhood hypophosphatasia (disorder) | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20
  444. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  445. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:childhood hypophosphatasia (disorder) | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  446. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  447. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20
  448. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:and hypogonadotropic hypogonadism
    n1=en:childhood hypophosphatasia (disorder) | n2=en:and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=20
  449. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:anterior plagiocephalies, synostotic
    n1=en:childhood hypophosphatasia (disorder) | n2=en:anterior plagiocephalies, synostotic | rel=r_associated | relid=0 | w=20
  450. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal recessive spastic paraplegia type 39
    n1=en:childhood hypophosphatasia (disorder) | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20
  451. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  452. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive
    n1=en:childhood hypophosphatasia (disorder) | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20
  453. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:braddock syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  454. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:brain calcification rajab type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  455. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:childhood hypophosphatasia (disorder) | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  456. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  457. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  458. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:cleft lip
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cleft lip | rel=r_associated | relid=0 | w=20
  459. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  460. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  461. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1h
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20
  462. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 2e
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20
  463. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20
  464. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20
  465. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if
    n1=en:childhood hypophosphatasia (disorder) | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20
  466. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  467. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:craniofacial ulnar renal syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20
  468. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:craniostenosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:craniostenosis | rel=r_associated | relid=0 | w=20
  469. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  470. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:deafness and myopia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  471. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:dental caries
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dental caries | rel=r_associated | relid=0 | w=20
  472. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  473. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20
  474. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Dubin-Johnson's syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Dubin-Johnson's syndrome | rel=r_associated | relid=0 | w=20
  475. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Dubin-Sprinz disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20
  476. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  477. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
  478. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:familial median cleft of upper and lower lip
    n1=en:childhood hypophosphatasia (disorder) | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  479. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  480. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  481. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20
  482. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  483. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:harelip
    n1=en:childhood hypophosphatasia (disorder) | n2=en:harelip | rel=r_associated | relid=0 | w=20
  484. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening
    n1=en:childhood hypophosphatasia (disorder) | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  485. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:hyperextensibility
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hyperextensibility | rel=r_associated | relid=0 | w=20
  486. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  487. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile
    n1=en:childhood hypophosphatasia (disorder) | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  488. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:I-cell disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20
  489. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  490. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:kallman syndrome with heart disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  491. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:keratoconus posticus
    n1=en:childhood hypophosphatasia (disorder) | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
  492. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:labial fissure
    n1=en:childhood hypophosphatasia (disorder) | n2=en:labial fissure | rel=r_associated | relid=0 | w=20
  493. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Laron syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Laron syndrome | rel=r_associated | relid=0 | w=20
  494. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa
    n1=en:childhood hypophosphatasia (disorder) | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  495. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Leroy's i-cell disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Leroy's i-cell disease | rel=r_associated | relid=0 | w=20
  496. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20
  497. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  498. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  499. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:manouvrier syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  500. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  501. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20
  502. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  503. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  504. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:moyamoya disease with early onset achalasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  505. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:mucopolysaccharidosis i
    n1=en:childhood hypophosphatasia (disorder) | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20
  506. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:multicore disease with mental retardation
    n1=en:childhood hypophosphatasia (disorder) | n2=en:multicore disease with mental retardation | rel=r_associated | relid=0 | w=20
  507. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:najjar syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  508. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Niemann-Pick disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20
  509. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:nystagmus
    n1=en:childhood hypophosphatasia (disorder) | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  510. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:oculocutaneous albinism type 6
    n1=en:childhood hypophosphatasia (disorder) | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20
  511. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:oxalosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:oxalosis | rel=r_associated | relid=0 | w=20
  512. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  513. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  514. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
  515. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:primary immunodeficiency syndrome due to p14 deficiency
    n1=en:childhood hypophosphatasia (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20
  516. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:proptosis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:proptosis | rel=r_associated | relid=0 | w=20
  517. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:protopsis
    n1=en:childhood hypophosphatasia (disorder) | n2=en:protopsis | rel=r_associated | relid=0 | w=20
  518. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  519. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Rieger anomaly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Rieger anomaly | rel=r_associated | relid=0 | w=20
  520. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  521. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:saprodontia
    n1=en:childhood hypophosphatasia (disorder) | n2=en:saprodontia | rel=r_associated | relid=0 | w=20
  522. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3
    n1=en:childhood hypophosphatasia (disorder) | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  523. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  524. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20
  525. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  526. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  527. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:tooth decay
    n1=en:childhood hypophosphatasia (disorder) | n2=en:tooth decay | rel=r_associated | relid=0 | w=20
  528. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:wolman's disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:wolman's disease | rel=r_associated | relid=0 | w=20
  529. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Wolman's disease
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  530. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  531. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  532. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> en:zellweger-like syndrome without peroxisomal anomaly
    n1=en:childhood hypophosphatasia (disorder) | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20
  533. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> exophtalmie
    n1=en:childhood hypophosphatasia (disorder) | n2=exophtalmie | rel=r_associated | relid=0 | w=20
  534. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> exophthalmie
    n1=en:childhood hypophosphatasia (disorder) | n2=exophthalmie | rel=r_associated | relid=0 | w=20
  535. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Fenn (diagramme de)
    n1=en:childhood hypophosphatasia (disorder) | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
  536. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> fente labiale
    n1=en:childhood hypophosphatasia (disorder) | n2=fente labiale | rel=r_associated | relid=0 | w=20
  537. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> fente labiopalatine et blépharophimosis
    n1=en:childhood hypophosphatasia (disorder) | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
  538. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique
    n1=en:childhood hypophosphatasia (disorder) | n2=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique | rel=r_associated | relid=0 | w=20
  539. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> fucosidose
    n1=en:childhood hypophosphatasia (disorder) | n2=fucosidose | rel=r_associated | relid=0 | w=20
  540. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:childhood hypophosphatasia (disorder) | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  541. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:childhood hypophosphatasia (disorder) | n2=histidinémie | rel=r_associated | relid=0 | w=20
  542. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> histiocytose sinusale hémophagocytaire
    n1=en:childhood hypophosphatasia (disorder) | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20
  543. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> homocarnosinose
    n1=en:childhood hypophosphatasia (disorder) | n2=homocarnosinose | rel=r_associated | relid=0 | w=20
  544. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire
    n1=en:childhood hypophosphatasia (disorder) | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  545. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive
    n1=en:childhood hypophosphatasia (disorder) | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  546. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:childhood hypophosphatasia (disorder) | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  547. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale
    n1=en:childhood hypophosphatasia (disorder) | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  548. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile
    n1=en:childhood hypophosphatasia (disorder) | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  549. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> insuffisance staturale
    n1=en:childhood hypophosphatasia (disorder) | n2=insuffisance staturale | rel=r_associated | relid=0 | w=20
  550. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:childhood hypophosphatasia (disorder) | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  551. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> kératocône postérieur-fente labiale-petite taille
    n1=en:childhood hypophosphatasia (disorder) | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
  552. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:childhood hypophosphatasia (disorder) | n2=leucinose | rel=r_associated | relid=0 | w=20
  553. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de dubin-johnson
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
  554. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Niemann-Pick
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20
  555. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  556. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  557. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  558. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de wolman
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  559. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Maladie de Wolman
    n1=en:childhood hypophosphatasia (disorder) | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20
  560. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Wolman
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  561. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  562. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  563. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  564. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:childhood hypophosphatasia (disorder) | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  565. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> mucolipidose II
    n1=en:childhood hypophosphatasia (disorder) | n2=mucolipidose II | rel=r_associated | relid=0 | w=20
  566. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> mucolipidose type ii
    n1=en:childhood hypophosphatasia (disorder) | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20
  567. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> mucolipidose type II
    n1=en:childhood hypophosphatasia (disorder) | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20
  568. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique
    n1=en:childhood hypophosphatasia (disorder) | n2=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | rel=r_associated | relid=0 | w=20
  569. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:childhood hypophosphatasia (disorder) | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  570. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:childhood hypophosphatasia (disorder) | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  571. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> oxalose
    n1=en:childhood hypophosphatasia (disorder) | n2=oxalose | rel=r_associated | relid=0 | w=20
  572. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> oxalose primitive
    n1=en:childhood hypophosphatasia (disorder) | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  573. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> oxaloses
    n1=en:childhood hypophosphatasia (disorder) | n2=oxaloses | rel=r_associated | relid=0 | w=20
  574. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> petite taille, hyperextensibilité, hernie et dépression oculaire
    n1=en:childhood hypophosphatasia (disorder) | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
  575. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> proptose
    n1=en:childhood hypophosphatasia (disorder) | n2=proptose | rel=r_associated | relid=0 | w=20
  576. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> proptosis
    n1=en:childhood hypophosphatasia (disorder) | n2=proptosis | rel=r_associated | relid=0 | w=20
  577. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> rétention des chylomicrons (maladie de la)
    n1=en:childhood hypophosphatasia (disorder) | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=20
  578. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> semialdéhyde succinique-déshydrogénase (déficit en)
    n1=en:childhood hypophosphatasia (disorder) | n2=semialdéhyde succinique-déshydrogénase (déficit en) | rel=r_associated | relid=0 | w=20
  579. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:childhood hypophosphatasia (disorder) | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  580. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson
    n1=en:childhood hypophosphatasia (disorder) | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  581. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson
    n1=en:childhood hypophosphatasia (disorder) | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  582. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:childhood hypophosphatasia (disorder) | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  583. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de synostose spondylo-carpo-tarsale
    n1=en:childhood hypophosphatasia (disorder) | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20
  584. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:childhood hypophosphatasia (disorder) | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  585. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de)
    n1=en:childhood hypophosphatasia (disorder) | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  586. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Wolman (maladie de)
    n1=en:childhood hypophosphatasia (disorder) | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  587. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:childhood hypophosphatasia (disorder) | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  588. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:childhood hypophosphatasia (disorder) | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  589. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:childhood hypophosphatasia (disorder) | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  590. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum
    n1=en:childhood hypophosphatasia (disorder) | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  591. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum
    n1=en:childhood hypophosphatasia (disorder) | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  592. en:childhood hypophosphatasia (disorder) -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire
    n1=en:childhood hypophosphatasia (disorder) | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
≈ 766 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 696 --> en:childhood hypophosphatasia (disorder)
    n1=en:maple syrup urine disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=696
  2. leucinose --- r_associated #0: 609.18 --> en:childhood hypophosphatasia (disorder)
    n1=leucinose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=609.18
  3. maladie du sirop d'érable --- r_associated #0: 604.37 --> en:childhood hypophosphatasia (disorder)
    n1=maladie du sirop d'érable | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=604.37
  4. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:childhood hypophosphatasia (disorder)
    n1=en:branched-chain ketoaciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=520
  5. craniosynostose --- r_associated #0: 280 --> en:childhood hypophosphatasia (disorder)
    n1=craniosynostose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=280
  6. en:classical maple syrup urine disease --- r_associated #0: 280 --> en:childhood hypophosphatasia (disorder)
    n1=en:classical maple syrup urine disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=280
  7. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 280 --> en:childhood hypophosphatasia (disorder)
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=280
  8. en:craniosynostosis --- r_associated #0: 279 --> en:childhood hypophosphatasia (disorder)
    n1=en:craniosynostosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=279
  9. crâniosténose --- r_associated #0: 278 --> en:childhood hypophosphatasia (disorder)
    n1=crâniosténose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=278
  10. crânio-sténose --- r_associated #0: 276 --> en:childhood hypophosphatasia (disorder)
    n1=crânio-sténose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=276
  11. crâniosynostose --- r_associated #0: 276 --> en:childhood hypophosphatasia (disorder)
    n1=crâniosynostose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=276
  12. déficit en céto-acide décarboxylase --- r_associated #0: 275 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en céto-acide décarboxylase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=275
  13. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 275 --> en:childhood hypophosphatasia (disorder)
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=275
  14. maladie des urines avec odeur de sirop erable --- r_associated #0: 270 --> en:childhood hypophosphatasia (disorder)
    n1=maladie des urines avec odeur de sirop erable | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=270
  15. en:infantile hypophosphatasia --- r_associated #0: 200 --> en:childhood hypophosphatasia (disorder)
    n1=en:infantile hypophosphatasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=200
  16. hypophosphatasie foetale --- r_associated #0: 199 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie foetale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=199
  17. hypophosphatasie infantile --- r_associated #0: 199 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie infantile | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=199
  18. craniosténose --- r_associated #0: 185 --> en:childhood hypophosphatasia (disorder)
    n1=craniosténose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=185
  19. en:pyruvate carboxylase deficiency --- r_associated #0: 180 --> en:childhood hypophosphatasia (disorder)
    n1=en:pyruvate carboxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=180
  20. en:walker-warburg syndrome --- r_associated #0: 180 --> en:childhood hypophosphatasia (disorder)
    n1=en:walker-warburg syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=180
  21. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Walker-Warburg | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=178
  22. déficit en pyruvate carboxylase --- r_associated #0: 177 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en pyruvate carboxylase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=177
  23. en:xeroderma pigmentosum --- r_associated #0: 175 --> en:childhood hypophosphatasia (disorder)
    n1=en:xeroderma pigmentosum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=175
  24. en:zellweger syndrome --- r_associated #0: 172 --> en:childhood hypophosphatasia (disorder)
    n1=en:zellweger syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=172
  25. xeroderma pigmentosum --- r_associated #0: 172 --> en:childhood hypophosphatasia (disorder)
    n1=xeroderma pigmentosum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=172
  26. en:Zellweger syndrome --- r_associated #0: 170 --> en:childhood hypophosphatasia (disorder)
    n1=en:Zellweger syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=170
  27. en:wolman disease --- r_associated #0: 163 --> en:childhood hypophosphatasia (disorder)
    n1=en:wolman disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=163
  28. maladie de Wolman --- r_associated #0: 161 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de Wolman | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=161
  29. hyperoxalurie primaire --- r_associated #0: 151 --> en:childhood hypophosphatasia (disorder)
    n1=hyperoxalurie primaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=151
  30. oxaloses --- r_associated #0: 151 --> en:childhood hypophosphatasia (disorder)
    n1=oxaloses | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=151
  31. hyperoxalurie primitive --- r_associated #0: 150 --> en:childhood hypophosphatasia (disorder)
    n1=hyperoxalurie primitive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=150
  32. en:primary hyperoxaluria --- r_associated #0: 148 --> en:childhood hypophosphatasia (disorder)
    n1=en:primary hyperoxaluria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=148
  33. oxalose primitive --- r_associated #0: 146 --> en:childhood hypophosphatasia (disorder)
    n1=oxalose primitive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=146
  34. oxalose --- r_associated #0: 140 --> en:childhood hypophosphatasia (disorder)
    n1=oxalose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=140
  35. en:exophthalmos --- r_associated #0: 131 --> en:childhood hypophosphatasia (disorder)
    n1=en:exophthalmos | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=131
  36. proptose --- r_associated #0: 131 --> en:childhood hypophosphatasia (disorder)
    n1=proptose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=131
  37. exophtalmie --- r_associated #0: 130 --> en:childhood hypophosphatasia (disorder)
    n1=exophtalmie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=130
  38. exophthalmie --- r_associated #0: 130 --> en:childhood hypophosphatasia (disorder)
    n1=exophthalmie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=130
  39. en:cytochrome-c oxidase deficiency --- r_associated #0: 114 --> en:childhood hypophosphatasia (disorder)
    n1=en:cytochrome-c oxidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=114
  40. déficit en cytochrome oxydase --- r_associated #0: 110 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en cytochrome oxydase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=110
  41. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en cytochrome-c oxydase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=95
  42. en:caries --- r_associated #0: 70 --> en:childhood hypophosphatasia (disorder)
    n1=en:caries | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=70
  43. caries --- r_associated #0: 68 --> en:childhood hypophosphatasia (disorder)
    n1=caries | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=68
  44. congénitale --- r_associated #0: 68 --> en:childhood hypophosphatasia (disorder)
    n1=congénitale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=68
  45. en:congenital --- r_associated #0: 66 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=66
  46. en:niemann-pick disease --- r_associated #0: 62 --> en:childhood hypophosphatasia (disorder)
    n1=en:niemann-pick disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=62
  47. en:dubin-johnson syndrome --- r_associated #0: 61 --> en:childhood hypophosphatasia (disorder)
    n1=en:dubin-johnson syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=61
  48. en:anterior plagiocephalies, synostotic --- r_associated #0: 60 --> en:childhood hypophosphatasia (disorder)
    n1=en:anterior plagiocephalies, synostotic | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=60
  49. syndrome de dubin-johnson --- r_associated #0: 60 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de dubin-johnson | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=60
  50. en:Niemann-Pick disease --- r_associated #0: 59 --> en:childhood hypophosphatasia (disorder)
    n1=en:Niemann-Pick disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=59
  51. en:mucopolysaccharidosis type i --- r_associated #0: 58 --> en:childhood hypophosphatasia (disorder)
    n1=en:mucopolysaccharidosis type i | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=58
  52. congenital --- r_associated #0: 57 --> en:childhood hypophosphatasia (disorder)
    n1=congenital | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=57
  53. Xeroderma pigmentosum --- r_associated #0: 55 --> en:childhood hypophosphatasia (disorder)
    n1=Xeroderma pigmentosum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=55
  54. en:mucopolysaccharidosis i --- r_associated #0: 55 --> en:childhood hypophosphatasia (disorder)
    n1=en:mucopolysaccharidosis i | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=55
  55. en:tay-sachs disease --- r_associated #0: 54 --> en:childhood hypophosphatasia (disorder)
    n1=en:tay-sachs disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=54
  56. congénital --- r_associated #0: 53 --> en:childhood hypophosphatasia (disorder)
    n1=congénital | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=53
  57. en:proptosis --- r_associated #0: 51 --> en:childhood hypophosphatasia (disorder)
    n1=en:proptosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=51
  58. carie dentaire --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=carie dentaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  59. en:Tay-Sachs disease --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=en:Tay-Sachs disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  60. en:Wolman's disease --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=en:Wolman's disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  61. kératocône postérieur-fente labiale-petite taille --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=kératocône postérieur-fente labiale-petite taille | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  62. syndrome de Dubin-Johnson --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Dubin-Johnson | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  63. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  64. xérodermite pigmentaire --- r_associated #0: 50 --> en:childhood hypophosphatasia (disorder)
    n1=xérodermite pigmentaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=50
  65. fente labiopalatine et blépharophimosis --- r_associated #0: 49 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiopalatine et blépharophimosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=49
  66. maladie de wolman --- r_associated #0: 48 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de wolman | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=48
  67. bec de lièvre --- r_associated #0: 47 --> en:childhood hypophosphatasia (disorder)
    n1=bec de lièvre | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=47
  68. en:cerebrotendinous xanthomatosis --- r_associated #0: 46 --> en:childhood hypophosphatasia (disorder)
    n1=en:cerebrotendinous xanthomatosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=46
  69. en:keratoconus posticus --- r_associated #0: 46 --> en:childhood hypophosphatasia (disorder)
    n1=en:keratoconus posticus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=46
  70. xanthomatose cérébro-tendineuse --- r_associated #0: 46 --> en:childhood hypophosphatasia (disorder)
    n1=xanthomatose cérébro-tendineuse | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=46
  71. xanthomatose cérébrotendineuse --- r_associated #0: 46 --> en:childhood hypophosphatasia (disorder)
    n1=xanthomatose cérébrotendineuse | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=46
  72. Carie dentaire --- r_associated #0: 45 --> en:childhood hypophosphatasia (disorder)
    n1=Carie dentaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=45
  73. en:cleft lip --- r_associated #0: 45 --> en:childhood hypophosphatasia (disorder)
    n1=en:cleft lip | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=45
  74. syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 44 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=44
  75. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  76. en:hereditary factor xii deficiency disease --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary factor xii deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  77. en:insulin growth factor i deficiency --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=en:insulin growth factor i deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  78. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  79. hérédité autosomale récessive --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=hérédité autosomale récessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  80. rétention des chylomicrons (maladie de la) --- r_associated #0: 43 --> en:childhood hypophosphatasia (disorder)
    n1=rétention des chylomicrons (maladie de la) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=43
  81. en:arterial tortuosity syndrome --- r_associated #0: 42 --> en:childhood hypophosphatasia (disorder)
    n1=en:arterial tortuosity syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42
  82. en:hyperandrogenism due to non-classic 21-hydroxylase deficiency --- r_associated #0: 42 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperandrogenism due to non-classic 21-hydroxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42
  83. en:renal dysplasia - limb defects syndrome --- r_associated #0: 42 --> en:childhood hypophosphatasia (disorder)
    n1=en:renal dysplasia - limb defects syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42
  84. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 42 --> en:childhood hypophosphatasia (disorder)
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42
  85. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 42 --> en:childhood hypophosphatasia (disorder)
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42
  86. en:alpl, ala99thr --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, ala99thr | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  87. en:autosomal recessive asexual dwarfism --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive asexual dwarfism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  88. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  89. en:familial hypoaldosteronism --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial hypoaldosteronism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  90. en:glutathione synthetase deficiency --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:glutathione synthetase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  91. en:papillon-lefevre syndrome --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:papillon-lefevre syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  92. en:rapadilino syndrome --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=en:rapadilino syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  93. fente labiale --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  94. petite taille, hyperextensibilité, hernie et dépression oculaire --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  95. sirop d'érable (urine à odeur de) --- r_associated #0: 41 --> en:childhood hypophosphatasia (disorder)
    n1=sirop d'érable (urine à odeur de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=41
  96. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=Walker-Warburg (syndrome de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  97. en:chylomicron retention disease --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:chylomicron retention disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  98. en:dental caries --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:dental caries | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  99. en:protopsis --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:protopsis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  100. en:saprodontia --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:saprodontia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  101. en:short stature --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:short stature | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  102. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  103. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  104. en:tooth decay --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=en:tooth decay | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  105. maladie de Niemann-Pick --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de Niemann-Pick | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  106. maladie de Tay-sachs --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de Tay-sachs | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  107. maladie de tay-sachs --- r_associated #0: 40 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de tay-sachs | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=40
  108. dysplasie craniodiaphysaire --- r_associated #0: 39 --> en:childhood hypophosphatasia (disorder)
    n1=dysplasie craniodiaphysaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  109. en:autosomal recessive inheritance --- r_associated #0: 39 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive inheritance | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  110. en:harelip --- r_associated #0: 39 --> en:childhood hypophosphatasia (disorder)
    n1=en:harelip | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  111. en:isovaleric acidemia --- r_associated #0: 39 --> en:childhood hypophosphatasia (disorder)
    n1=en:isovaleric acidemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  112. en:persistent mullerian duct syndrome --- r_associated #0: 39 --> en:childhood hypophosphatasia (disorder)
    n1=en:persistent mullerian duct syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=39
  113. en:behrens baumann dust syndrome --- r_associated #0: 38 --> en:childhood hypophosphatasia (disorder)
    n1=en:behrens baumann dust syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=38
  114. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 38 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=38
  115. en:laurence-moon syndrome --- r_associated #0: 38 --> en:childhood hypophosphatasia (disorder)
    n1=en:laurence-moon syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=38
  116. myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique --- r_associated #0: 38 --> en:childhood hypophosphatasia (disorder)
    n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=38
  117. en:craniodiaphyseal dysplasia --- r_associated #0: 37 --> en:childhood hypophosphatasia (disorder)
    n1=en:craniodiaphyseal dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=37
  118. en:generalized peeling skin syndrome --- r_associated #0: 37 --> en:childhood hypophosphatasia (disorder)
    n1=en:generalized peeling skin syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=37
  119. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 37 --> en:childhood hypophosphatasia (disorder)
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=37
  120. en:naxos disease --- r_associated #0: 37 --> en:childhood hypophosphatasia (disorder)
    n1=en:naxos disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=37
  121. déficit en prolidase --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en prolidase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  122. en:bowen-conradi syndrome --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=en:bowen-conradi syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  123. en:deficiency of glucosyltransferase 1 --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=en:deficiency of glucosyltransferase 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  124. en:prolidase deficiency --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=en:prolidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  125. histiocytose sinusale hémophagocytaire --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=histiocytose sinusale hémophagocytaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  126. syndrome de Laurence-Moon --- r_associated #0: 36 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Laurence-Moon | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=36
  127. Bec de lièvre --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=Bec de lièvre | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  128. Wolman (maladie de) --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=Wolman (maladie de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  129. acrodermatite entéropathique --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=acrodermatite entéropathique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  130. en:acid phosphatase deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:acid phosphatase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  131. en:acrocallosal syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:acrocallosal syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  132. en:acrodermatitis enteropathica --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:acrodermatitis enteropathica | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  133. en:argininosuccinic aciduria --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:argininosuccinic aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  134. en:ataxia with vitamin e deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:ataxia with vitamin e deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  135. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  136. en:bestrophinopathy, autosomal recessive --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:bestrophinopathy, autosomal recessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  137. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  138. en:brown-vialetto-van laere syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:brown-vialetto-van laere syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  139. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  140. en:circulating enzyme deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:circulating enzyme deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  141. en:citrin deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:citrin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  142. en:congenital bowing of long bone --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital bowing of long bone | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  143. en:craniofacial ulnar renal syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:craniofacial ulnar renal syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  144. en:crigler-najjar syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:crigler-najjar syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  145. en:deafness, progressive, with stapes fixation --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:deafness, progressive, with stapes fixation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  146. en:deficiency of steryl-sulfatase --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:deficiency of steryl-sulfatase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  147. en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  148. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  149. en:familial acantholysis --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial acantholysis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  150. en:ferrochelatase deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:ferrochelatase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  151. en:glutamate formiminotransferase deficiency --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:glutamate formiminotransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  152. en:gurrieri sammito bellussi syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:gurrieri sammito bellussi syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  153. en:heart defects limb shortening --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:heart defects limb shortening | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  154. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  155. en:hereditary factor xi deficiency disease --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary factor xi deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  156. en:hereditary fructose intolerance --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary fructose intolerance | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  157. en:histidinemia --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:histidinemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  158. en:hyperimmunoglobulin e syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperimmunoglobulin e syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  159. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  160. en:hypomagnesemia 1, intestinal --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypomagnesemia 1, intestinal | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  161. en:hypophosphatasia, infantile, glu174lys (allelic variant) --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypophosphatasia, infantile, glu174lys (allelic variant) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  162. en:infantile globoid cell leukodystrophy --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:infantile globoid cell leukodystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  163. en:knobloch syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:knobloch syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  164. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  165. en:maroteaux-lamy syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:maroteaux-lamy syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  166. en:microcephaly, amish type (disorder) --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:microcephaly, amish type (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  167. en:netherton syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:netherton syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  168. en:ornithine carbamoyltransferase deficiency disease --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  169. en:pelizaeus merzbacher like disease --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:pelizaeus merzbacher like disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  170. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  171. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  172. en:robinow-like syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:robinow-like syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  173. en:sly syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:sly syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  174. en:spondylo-ocular syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondylo-ocular syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  175. en:thomas syndrome --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:thomas syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  176. en:tyrosinemia, type iii --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=en:tyrosinemia, type iii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  177. hypophosphatasie juvénile --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie juvénile | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  178. intolérance au fructose --- r_associated #0: 35 --> en:childhood hypophosphatasia (disorder)
    n1=intolérance au fructose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  179. en:2-hydroxyglutaric aciduria --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:2-hydroxyglutaric aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  180. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  181. en:3-methylglutaconic aciduria type iv --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:3-methylglutaconic aciduria type iv | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  182. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  183. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  184. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  185. en:allgrove syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:allgrove syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  186. en:alpl, asp277ala --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, asp277ala | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  187. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  188. en:ataxia telangiectasia syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:ataxia telangiectasia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  189. en:autosomal recessive primary microcephaly --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive primary microcephaly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  190. en:basal ganglia disease, biotin-responsive --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:basal ganglia disease, biotin-responsive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  191. en:behr syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:behr syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  192. en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  193. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  194. en:congenital disorder of glycosylation, type if --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation, type if | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  195. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  196. en:congenital leptin deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital leptin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  197. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  198. en:cooper jabs syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:cooper jabs syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  199. en:corpus callosum agenesis neuronopathy --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:corpus callosum agenesis neuronopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  200. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  201. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  202. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  203. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  204. en:fucosidosis --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:fucosidosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  205. en:hall riggs syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:hall riggs syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  206. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  207. en:hereditary factor x deficiency disease --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary factor x deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  208. en:hnsha due to aldolase a deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to aldolase a deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  209. en:hyperphosphatasia with mental retardation --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperphosphatasia with mental retardation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  210. en:isolated hyperchlorhidrosis --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:isolated hyperchlorhidrosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  211. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  212. en:leucinosis --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:leucinosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  213. en:lipoid congenital adrenal hyperplasia --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:lipoid congenital adrenal hyperplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  214. en:long narrow head --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:long narrow head | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  215. en:low alkaline phosphatase --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:low alkaline phosphatase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  216. en:macdermot winter syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:macdermot winter syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  217. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  218. en:morm syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:morm syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  219. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  220. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  221. en:neuraminidase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:neuraminidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  222. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  223. en:odontohypophosphatasia (disorder) --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:odontohypophosphatasia (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  224. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  225. en:peeling skin syndrome, acral type --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:peeling skin syndrome, acral type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  226. en:pseudocholinesterase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:pseudocholinesterase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  227. en:saito kuba tsuruta syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:saito kuba tsuruta syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  228. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  229. en:sitosterolemia with xanthomatosis --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:sitosterolemia with xanthomatosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  230. en:sonoda syndrome --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:sonoda syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  231. en:urocanase deficiency --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:urocanase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  232. en:xanthinuria, type i --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:xanthinuria, type i | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  233. en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 34 --> en:childhood hypophosphatasia (disorder)
    n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=34
  234. Fenn (diagramme de) --- r_associated #0: 33 --> en:childhood hypophosphatasia (disorder)
    n1=Fenn (diagramme de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=33
  235. en:hypophosphatasia infantile --- r_associated #0: 33 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypophosphatasia infantile | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=33
  236. en:maple-tree syrup disease --- r_associated #0: 33 --> en:childhood hypophosphatasia (disorder)
    n1=en:maple-tree syrup disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=33
  237. nystagmus congénital isolé --- r_associated #0: 33 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus congénital isolé | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=33
  238. en:alkaptonuria --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:alkaptonuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  239. en:alpl, ala176thr --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, ala176thr | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  240. en:alpl, gly232val --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, gly232val | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  241. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  242. en:anauxetic dysplasia --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:anauxetic dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  243. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  244. en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  245. en:bothnia retinal dystrophy --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:bothnia retinal dystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  246. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  247. en:congenital analbuminemia --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital analbuminemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  248. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  249. en:congenital disorder of glycosylation type 1h --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type 1h | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  250. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  251. en:cryptophthalmos syndrome --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:cryptophthalmos syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  252. en:cutis laxa, autosomal recessive --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:cutis laxa, autosomal recessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  253. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  254. en:desmosterolosis --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:desmosterolosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  255. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  256. en:ehlers-danlos syndrome, type vi --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:ehlers-danlos syndrome, type vi | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  257. en:ethanolaminosis --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:ethanolaminosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  258. en:kallman syndrome with heart disease --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:kallman syndrome with heart disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  259. en:laron syndrome --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:laron syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  260. en:lethal congenital contracture syndrome 1 --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:lethal congenital contracture syndrome 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  261. en:macular corneal dystrophy --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:macular corneal dystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  262. en:mannosidosis --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:mannosidosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  263. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  264. en:neuroacanthocytosis --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:neuroacanthocytosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  265. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  266. en:otoonychoperoneal syndrome --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:otoonychoperoneal syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  267. en:pelviscapular dysplasia --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:pelviscapular dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  268. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  269. en:prolonged electroretinal response suppression --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:prolonged electroretinal response suppression | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  270. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  271. en:transcobalamin ii deficiency --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:transcobalamin ii deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  272. en:ugt1a1*28 polymorphism --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=en:ugt1a1*28 polymorphism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  273. maladie lysosomique de surcharge --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=maladie lysosomique de surcharge | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  274. neuro-acanthocytose --- r_associated #0: 32 --> en:childhood hypophosphatasia (disorder)
    n1=neuro-acanthocytose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=32
  275. déficit en neuraminidase --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en neuraminidase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  276. en:21-hydroxylase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:21-hydroxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  277. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  278. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  279. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  280. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  281. en:autosomal recessive scid --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive scid | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  282. en:bardet-biedl syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:bardet-biedl syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  283. en:chitty hall baraitser syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:chitty hall baraitser syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  284. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  285. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  286. en:dicarboxylicaminoaciduria --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:dicarboxylicaminoaciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  287. en:donnai-barrow syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:donnai-barrow syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  288. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  289. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  290. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  291. en:hydroxykynureninuria --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:hydroxykynureninuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  292. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  293. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  294. en:leukotriene c4 synthase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:leukotriene c4 synthase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  295. en:majeed syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:majeed syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  296. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  297. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  298. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  299. en:n-acetylglutamate synthase deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:n-acetylglutamate synthase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  300. en:najjar syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:najjar syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  301. en:nonaka myopathy --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:nonaka myopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  302. en:north american indian childhood cirrhosis --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:north american indian childhood cirrhosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  303. en:northern epilepsy syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:northern epilepsy syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  304. en:oculocutaneous albinism type 6 --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:oculocutaneous albinism type 6 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  305. en:phosphorus metabolic disorder --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:phosphorus metabolic disorder | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  306. en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  307. en:smith-mccort dysplasia --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:smith-mccort dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  308. en:waardenburg anophthalmia syndrome --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:waardenburg anophthalmia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  309. en:werdnig-hoffmann disease --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=en:werdnig-hoffmann disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  310. fucosidose --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=fucosidose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  311. histidinémie --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=histidinémie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  312. homocarnosinose --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=homocarnosinose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  313. mucolipidose II --- r_associated #0: 31 --> en:childhood hypophosphatasia (disorder)
    n1=mucolipidose II | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31
  314. déficit congénital en mégacaryocytes --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=déficit congénital en mégacaryocytes | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  315. en:17 alpha-hydroxyprogesterone aldolase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:17 alpha-hydroxyprogesterone aldolase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  316. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  317. en:I-cell disease --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:I-cell disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  318. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  319. en:alpl, gly145val --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, gly145val | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  320. en:argininemia --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:argininemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  321. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  322. en:autosomal recessive ocular albinism --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive ocular albinism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  323. en:biotinidase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:biotinidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  324. en:congenital adrenal hyperplasia --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital adrenal hyperplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  325. en:congenital disorder of glycosylation type id --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type id | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  326. en:congenital transferrin deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital transferrin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  327. en:deficiency of fructokinase --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:deficiency of fructokinase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  328. en:diaphanospondylodysostosis --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:diaphanospondylodysostosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  329. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  330. en:enterokinase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:enterokinase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  331. en:gamma-glutamyltransferase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:gamma-glutamyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  332. en:genu varum --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:genu varum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  333. en:glutamate-cysteine ligase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:glutamate-cysteine ligase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  334. en:glutathione s-transferase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:glutathione s-transferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  335. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  336. en:glycogen storage disease type i --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:glycogen storage disease type i | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  337. en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  338. en:hereditary xanthinuria --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary xanthinuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  339. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  340. en:hypospadias-mental retardation syndrome --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypospadias-mental retardation syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  341. en:i-cell disease --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:i-cell disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  342. en:increased aromatase activity --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:increased aromatase activity | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  343. en:lipoprotein glomerulopathy --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:lipoprotein glomerulopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  344. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  345. en:muscle amp deaminase deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:muscle amp deaminase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  346. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  347. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  348. en:presentey anomaly --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:presentey anomaly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  349. en:rachitic skeletal changes --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:rachitic skeletal changes | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  350. en:retinitis punctata albescens (disorder) --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:retinitis punctata albescens (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  351. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  352. hyperplasie congénitale des surrénales --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=hyperplasie congénitale des surrénales | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  353. insuffisance staturale --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=insuffisance staturale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  354. maladie de Tay-Sachs --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de Tay-Sachs | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  355. mucolipidose type II --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=mucolipidose type II | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  356. mucolipidose type ii --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=mucolipidose type ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  357. proptosis --- r_associated #0: 30 --> en:childhood hypophosphatasia (disorder)
    n1=proptosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=30
  358. acrodermatitis enteropathica --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=acrodermatitis enteropathica | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  359. en:Dubin-Sprinz disease --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:Dubin-Sprinz disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  360. en:alpha-fetoprotein deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpha-fetoprotein deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  361. en:alpl, arg272cys --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, arg272cys | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  362. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  363. en:bamforth syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:bamforth syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  364. en:carnitine palmitoyltransferase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:carnitine palmitoyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  365. en:cerebellar ataxia, cayman type --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:cerebellar ataxia, cayman type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  366. en:chondrodysplasia punctata syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:chondrodysplasia punctata syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  367. en:cohen syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:cohen syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  368. en:congenital disorder of glycosylation type 2e --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type 2e | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  369. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  370. en:craniostenosis --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:craniostenosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  371. en:disorder due to cytochrome p450 enzyme variant --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:disorder due to cytochrome p450 enzyme variant | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  372. en:familial renal iminoglycinuria --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial renal iminoglycinuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  373. en:fryns macrocephaly --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:fryns macrocephaly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  374. en:geroderma osteodysplastica --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:geroderma osteodysplastica | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  375. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  376. en:hereditary orotic aciduria --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary orotic aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  377. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  378. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  379. en:isaacs syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:isaacs syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  380. en:jervell and lange nielsen syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:jervell and lange nielsen syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  381. en:labial fissure --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:labial fissure | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  382. en:lactose intolerance, adult type --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:lactose intolerance, adult type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  383. en:methionine adenosyltransferase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:methionine adenosyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  384. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  385. en:morquio syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:morquio syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  386. en:orotic aciduria --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:orotic aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  387. en:phenylketonuria ii --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:phenylketonuria ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  388. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  389. en:porphobilinogen synthase deficiency --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:porphobilinogen synthase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  390. en:propionic acidemia --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:propionic acidemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  391. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  392. en:reardon hall slaney syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:reardon hall slaney syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  393. en:richards-rundle syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:richards-rundle syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  394. en:skin dimple over apex of long bone angulation --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:skin dimple over apex of long bone angulation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  395. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  396. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  397. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  398. en:tyrosinemia type ii --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:tyrosinemia type ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  399. en:valinemia --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:valinemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  400. en:wolman's disease --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=en:wolman's disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  401. hypophosphatasie de l'enfant --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie de l'enfant | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  402. maladie de dubin-johnson --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de dubin-johnson | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  403. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 29 --> en:childhood hypophosphatasia (disorder)
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=29
  404. diabète phosphaté familial chronique --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=diabète phosphaté familial chronique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  405. en:acrorenal mandibular syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:acrorenal mandibular syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  406. en:aminoacylase 1 deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:aminoacylase 1 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  407. en:aminomethyltransferase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:aminomethyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  408. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  409. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  410. en:atrophoderma vermiculatum --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:atrophoderma vermiculatum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  411. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  412. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  413. en:becker generalized myotonia --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:becker generalized myotonia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  414. en:brody myopathy --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:brody myopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  415. en:combined malonic and methylmalonic aciduria --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:combined malonic and methylmalonic aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  416. en:congenital disorder of glycosylation type ic --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type ic | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  417. en:congenital disorder of glycosylation type ig --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type ig | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  418. en:crisponi syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:crisponi syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  419. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  420. en:dihydropyrimidinase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:dihydropyrimidinase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  421. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  422. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  423. en:factor v and factor viii, combined deficiency of --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:factor v and factor viii, combined deficiency of | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  424. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  425. en:fronto-facio-nasal dysplasia --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:fronto-facio-nasal dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  426. en:glycogen storage disease type x --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:glycogen storage disease type x | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  427. en:hmg-coa lyase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:hmg-coa lyase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  428. en:homocarnosinosis --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:homocarnosinosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  429. en:hyperprolinemia type 1 --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperprolinemia type 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  430. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  431. en:intestinal epithelial dysplasia --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:intestinal epithelial dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  432. en:isolated hypoplasia of the right ventricle --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:isolated hypoplasia of the right ventricle | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  433. en:lactase deficiency, congenital --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:lactase deficiency, congenital | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  434. en:late-onset junctional epidermolysis bullosa --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:late-onset junctional epidermolysis bullosa | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  435. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  436. en:lysosomal storage disease --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:lysosomal storage disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  437. en:manouvrier syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:manouvrier syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  438. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  439. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  440. en:neutral lipid storage disease with myopathy --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:neutral lipid storage disease with myopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  441. en:pancreatic alpha-amylase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:pancreatic alpha-amylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  442. en:pancreatic colipase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:pancreatic colipase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  443. en:phosphate diabetes --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:phosphate diabetes | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  444. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  445. en:rachitic rosary --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:rachitic rosary | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  446. en:sanfilippo syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:sanfilippo syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  447. en:sarcosinemia --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:sarcosinemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  448. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  449. en:specific enzyme deficiency --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:specific enzyme deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  450. en:split-hand/foot malformation 3 --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:split-hand/foot malformation 3 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  451. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  452. en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  453. en:tungland bellman syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:tungland bellman syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  454. en:type ii acrocephalopolysyndactyly --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:type ii acrocephalopolysyndactyly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  455. en:warsaw breakage syndrome --- r_associated #0: 28 --> en:childhood hypophosphatasia (disorder)
    n1=en:warsaw breakage syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28
  456. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  457. en:17-beta-hydroxysteroid dehydrogenase 3 deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  458. en:5-oxoprolinase deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:5-oxoprolinase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  459. en:acquired lactase deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:acquired lactase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  460. en:acyl-coa dehydrogenase deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:acyl-coa dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  461. en:alpha, alpha-trehalase deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpha, alpha-trehalase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  462. en:arakawa syndrome ii --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:arakawa syndrome ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  463. en:autosomal recessive ichthyosis --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive ichthyosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  464. en:braddock syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:braddock syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  465. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  466. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  467. en:characteristic metaphyseal radiolucency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:characteristic metaphyseal radiolucency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  468. en:classical phenylketonuria --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:classical phenylketonuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  469. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  470. en:congenital disorder of glycosylation type ia --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type ia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  471. en:congenital disorder of glycosylation type ie --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital disorder of glycosylation type ie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  472. en:deafness and myopia syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:deafness and myopia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  473. en:deafness, sensorineural, and male infertility --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:deafness, sensorineural, and male infertility | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  474. en:deficiency in enzyme complexes of mitochondrial respiratory chain --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:deficiency in enzyme complexes of mitochondrial respiratory chain | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  475. en:familial median cleft of upper and lower lip --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:familial median cleft of upper and lower lip | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  476. en:hepatolenticular degeneration --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:hepatolenticular degeneration | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  477. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  478. en:hyperprolinemia type 2 --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperprolinemia type 2 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  479. en:hypomandibular faciocranial dysostosis --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypomandibular faciocranial dysostosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  480. en:hypomyelination and congenital cataract --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypomyelination and congenital cataract | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  481. en:kuskokwim disease --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:kuskokwim disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  482. en:lethal congenital contracture syndrome 2 --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:lethal congenital contracture syndrome 2 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  483. en:lethal larsen-like syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:lethal larsen-like syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  484. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  485. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  486. en:moyamoya disease with early onset achalasia --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:moyamoya disease with early onset achalasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  487. en:multicore disease with mental retardation --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:multicore disease with mental retardation | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  488. en:multiple sulfatase deficiency disease --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:multiple sulfatase deficiency disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  489. en:oxalosis --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:oxalosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  490. en:severe early childhood onset retinal dystrophy --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:severe early childhood onset retinal dystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  491. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  492. en:spondyloenchondrodysplasia --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondyloenchondrodysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  493. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  494. en:thyroid dyshormonogenesis 4 --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:thyroid dyshormonogenesis 4 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  495. en:trichohepatoenteric syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:trichohepatoenteric syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  496. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 27 --> en:childhood hypophosphatasia (disorder)
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  497. Maladie de Wolman --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=Maladie de Wolman | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  498. bébé bronzé (syndrome du) --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=bébé bronzé (syndrome du) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  499. en:Dubin-Johnson's syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:Dubin-Johnson's syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  500. en:Laron syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:Laron syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  501. en:Leroy's i-cell disease --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:Leroy's i-cell disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  502. en:Rieger anomaly --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:Rieger anomaly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  503. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  504. en:al awadi syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:al awadi syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  505. en:aldosterone synthase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:aldosterone synthase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  506. en:alpha-1 antitrypsin deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpha-1 antitrypsin deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  507. en:alpl, arg119his --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:alpl, arg119his | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  508. en:and hypogonadotropic hypogonadism --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:and hypogonadotropic hypogonadism | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  509. en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:autosomal recessive sideroblastic anemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  510. en:brachydactyly syndrome type b --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:brachydactyly syndrome type b | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  511. en:brain calcification rajab type --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:brain calcification rajab type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  512. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  513. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  514. en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:charcot-marie-tooth disease type 4 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  515. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  516. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  517. en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:dystonia, dopa-responsive, due to sepiapterin reductase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  518. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  519. en:elevated plasma and urine inorganic pyrophosphate (ppi) --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:elevated plasma and urine inorganic pyrophosphate (ppi) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  520. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  521. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  522. en:fountain syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:fountain syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  523. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  524. en:gracile syndrome (disorder) --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:gracile syndrome (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  525. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  526. en:hyperextensibility --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperextensibility | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  527. en:hypokalemia, familial --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypokalemia, familial | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  528. en:hypophosphatasia --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:hypophosphatasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  529. en:jankovic rivera syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:jankovic rivera syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  530. en:joubert syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:joubert syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  531. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  532. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  533. en:marles greenberg persaud syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:marles greenberg persaud syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  534. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  535. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  536. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  537. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  538. en:microcephaly-capillary malformation syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  539. en:muscle d-lactate dehydrogenase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:muscle d-lactate dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  540. en:nathalie syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:nathalie syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  541. en:neonatal progeroid syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:neonatal progeroid syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  542. en:nystagmus --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:nystagmus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  543. en:oculocutaneous albinism type 4 --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:oculocutaneous albinism type 4 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  544. en:pili torti onychodysplasia syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:pili torti onychodysplasia syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  545. en:pseudotrisomy 13 syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  546. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  547. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  548. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  549. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  550. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  551. en:sulfite oxidase deficiency --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:sulfite oxidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  552. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  553. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  554. en:uv-sensitive syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:uv-sensitive syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  555. en:verloes bourguignon syndrome --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=en:verloes bourguignon syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  556. fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  557. hypophosphatasie, forme juvénile --- r_associated #0: 26 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie, forme juvénile | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  558. en:Laurence-Moon's syndrome --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:Laurence-Moon's syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  559. en:baller-gerold syndrome --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:baller-gerold syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  560. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  561. en:hernia --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:hernia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  562. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  563. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  564. en:pentosuria --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:pentosuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  565. en:premature deciduous tooth loss (less than five years of age) --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:premature deciduous tooth loss (less than five years of age) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  566. en:tetra-amelia autosomal recessive --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:tetra-amelia autosomal recessive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  567. en:waddling gait --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=en:waddling gait | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  568. kératocône posticus --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=kératocône posticus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  569. proptose oculaire --- r_associated #0: 25 --> en:childhood hypophosphatasia (disorder)
    n1=proptose oculaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25
  570. adénite sinusale cytophagique --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=adénite sinusale cytophagique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  571. en:allanson pantzar mcleod syndrome --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:allanson pantzar mcleod syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  572. en:and teething delay --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:and teething delay | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  573. en:citrullinemia --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:citrullinemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  574. en:disorder due to n-acetyltransferase enzyme variant --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:disorder due to n-acetyltransferase enzyme variant | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  575. en:frontal bossing --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:frontal bossing | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  576. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  577. en:histidinaemia --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:histidinaemia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  578. en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 24 --> en:childhood hypophosphatasia (disorder)
    n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  579. Maladie de Tay-Sachs --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=Maladie de Tay-Sachs | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  580. déficit en biotinidase --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en biotinidase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  581. en:Nathalie syndrome --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:Nathalie syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  582. en:cleft palate --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:cleft palate | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  583. en:ear, patella, short stature syndrome --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:ear, patella, short stature syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  584. en:lecithin acyltransferase deficiency --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:lecithin acyltransferase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  585. en:ocular depression --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:ocular depression | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  586. en:tyrosinemia type II --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:tyrosinemia type II | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  587. en:zinc-deficiency type --- r_associated #0: 23 --> en:childhood hypophosphatasia (disorder)
    n1=en:zinc-deficiency type | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  588. en:adrenal gland hyperplasia ii --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:adrenal gland hyperplasia ii | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  589. en:adult hypophosphatasia (disorder) --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:adult hypophosphatasia (disorder) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  590. en:alstrom syndrome --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:alstrom syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  591. en:cystinosis --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:cystinosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  592. en:intestinal disaccharidase deficiency --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:intestinal disaccharidase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  593. en:odontonecrosis --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:odontonecrosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  594. en:periodontitis co-occurrent with hypophosphatasia --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:periodontitis co-occurrent with hypophosphatasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  595. en:presentation after 6 months --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=en:presentation after 6 months | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  596. mucopolysaccharidose de type I --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=mucopolysaccharidose de type I | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  597. xanthique (lithiase) --- r_associated #0: 22 --> en:childhood hypophosphatasia (disorder)
    n1=xanthique (lithiase) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=22
  598. acidurie argininosuccinique --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=acidurie argininosuccinique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  599. acidémie isovalérique --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=acidémie isovalérique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  600. alcaptonurie --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=alcaptonurie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  601. argininémie --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=argininémie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  602. contractures congénitales et arachnodactylie --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=contractures congénitales et arachnodactylie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  603. cétoacidurie à chaînes ramifiées --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=cétoacidurie à chaînes ramifiées | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  604. déficit en sulfite-oxydase --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en sulfite-oxydase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  605. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=déficit enzymatique partiel de la surrénale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  606. en:albinotic fundus --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:albinotic fundus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  607. en:aspartylglycosaminuria --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:aspartylglycosaminuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  608. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  609. en:beta-aminoisobutyricaciduria --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:beta-aminoisobutyricaciduria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  610. en:childhood --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:childhood | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  611. en:kaufman-mckusick syndrome --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:kaufman-mckusick syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  612. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  613. en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  614. en:myopathy --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:myopathy | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  615. en:palate-blepharophimosis --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:palate-blepharophimosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  616. en:peters-plus syndrome --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:peters-plus syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  617. en:pyle metaphyseal dysplasia --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:pyle metaphyseal dysplasia | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  618. en:seizure --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:seizure | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  619. en:type a 14 --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:type a 14 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  620. en:walking delay --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=en:walking delay | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  621. idiosyncrasie au fructose --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=idiosyncrasie au fructose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  622. mannosidose --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=mannosidose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  623. mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=mucopolysaccharidose de type 1 | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  624. syndrome de Zellweger --- r_associated #0: 21 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Zellweger | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=21
  625. syndrome de Warburg --- r_associated #0: 16 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Warburg | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=16
  626. Carhart (encoche de) --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Carhart (encoche de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  627. Fuchs (syndrome de) --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Fuchs (syndrome de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  628. His (faisceau de) --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=His (faisceau de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  629. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Hyperplasie congénitale des surrénales | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  630. Intolérance au fructose --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Intolérance au fructose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  631. Maladie de Niemann-Pick --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Maladie de Niemann-Pick | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  632. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=Syndrome de Walker-Warburg | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  633. fente labio-palatine --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=fente labio-palatine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  634. fente labiopalatine --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiopalatine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  635. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  636. hypophosphatasie --- r_associated #0: 15 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=15
  637. BEC DE LIEVRE --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=BEC DE LIEVRE | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  638. CONGÉNITALE --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=CONGÉNITALE | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  639. Caries --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Caries | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  640. Craniosynostose --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Craniosynostose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  641. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Dubin-Johnson (syndrome de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  642. Exophtalmie --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Exophtalmie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  643. Fucosidose --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Fucosidose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  644. Histidinémie --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Histidinémie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  645. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Laurence-Moon (syndrome de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  646. Manning (score de) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Manning (score de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  647. Mannosidose --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Mannosidose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  648. Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=Niemann-Pick (maladie de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  649. alcalose métabolique (classification) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=alcalose métabolique (classification) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  650. bec de corbin --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=bec de corbin | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  651. bec de cuiller --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=bec de cuiller | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  652. bec de la prostate --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=bec de la prostate | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  653. bec de la rotule --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=bec de la rotule | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  654. bébé collodion --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=bébé collodion | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  655. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=cornée et tyrosinose de type II | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  656. division palatine --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=division palatine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  657. déficit en phosphatases alcalines --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=déficit en phosphatases alcalines | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  658. en:Carhart's notch --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:Carhart's notch | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  659. en:Fenn's diagram --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:Fenn's diagram | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  660. en:HHH syndrome --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:HHH syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  661. en:Tay Sachs' disease --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:Tay Sachs' disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  662. en:alcaptonuria --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:alcaptonuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  663. en:bony frailty with craniostenosis --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:bony frailty with craniostenosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  664. en:bronze baby syndrome --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:bronze baby syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  665. en:contractural arachnodactyly --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:contractural arachnodactyly | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  666. en:dental cavity --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:dental cavity | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  667. en:dental decay --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:dental decay | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  668. en:homogentisuria --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:homogentisuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  669. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  670. en:labiopalatine cleft --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:labiopalatine cleft | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  671. en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:phosphatide thesaurismosis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  672. en:xanthine lithiasis --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=en:xanthine lithiasis | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  673. fente cérébrale de Bichat --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente cérébrale de Bichat | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  674. fente de Larrey --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente de Larrey | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  675. fente de la glotte --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente de la glotte | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  676. fente foetale --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente foetale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  677. fente hypophysaire --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente hypophysaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  678. fente interaryténoïdienne --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente interaryténoïdienne | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  679. fente interfessière --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente interfessière | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  680. fente labiopalatine et kystes muqueux de la lèvre inférieure --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  681. fente labiopalatine, ectropion et dents coniques --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiopalatine, ectropion et dents coniques | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  682. fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  683. fente palatine --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fente palatine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  684. fissure palatine --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fissure palatine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  685. fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique; --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fragilité osseuse avec craniosynostose, exophtalmie, hydrocéphalie et faciès caractéristique; | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  686. fénotérol --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=fénotérol | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  687. genu varum --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=genu varum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  688. hypophosphatasies --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=hypophosphatasies | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  689. maladie de niemann-pick --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=maladie de niemann-pick | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  690. myopathie --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=myopathie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  691. nanisme de type Laron --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=nanisme de type Laron | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  692. neuraminidase (déficit en) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=neuraminidase (déficit en) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  693. nystagmus --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  694. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus héréditaire vertical | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  695. nystagmus lié au sexe --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus lié au sexe | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  696. nystagmus myoclonies --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus myoclonies | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  697. prolidase (déficit en) --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=prolidase (déficit en) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  698. rétention hydrochlorurée sodique --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétention hydrochlorurée sodique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  699. rétention membraneuse --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétention membraneuse | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  700. rétention placentaire --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétention placentaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  701. rétention placentaire du postabortum --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétention placentaire du postabortum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  702. rétention sudorale --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétention sudorale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  703. rétentionniste --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=rétentionniste | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  704. sirtuine --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=sirtuine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  705. sisi-test --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=sisi-test | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  706. sismothérapie --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=sismothérapie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  707. syndrome de Nathalie --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Nathalie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  708. syndrome de Rathbun --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Rathbun | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  709. syndrome de warburg --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de warburg | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  710. syndrome de zellweger --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de zellweger | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  711. xanthomatose familiale primitive --- r_associated #0: 10 --> en:childhood hypophosphatasia (disorder)
    n1=xanthomatose familiale primitive | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=10
  712. Fente labiale --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=Fente labiale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  713. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=Tay-Sachs (maladie de) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  714. bec de perroquet --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=bec de perroquet | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  715. bec du cuboïde --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=bec du cuboïde | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  716. bec du sphénoïde --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=bec du sphénoïde | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  717. bec scléral --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=bec scléral | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  718. bécégite --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=bécégite | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  719. caricine --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=caricine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  720. en:Sachs' disease --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=en:Sachs' disease | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  721. faisceau de His --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=faisceau de His | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  722. fuchsine --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=fuchsine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  723. fucose --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=fucose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  724. fucosidase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=fucosidase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  725. fucoside --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=fucoside | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  726. histaminergie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminergie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  727. histaminergique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminergique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  728. histaminique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  729. histaminolibération --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminolibération | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  730. histaminolytique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminolytique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  731. histaminopexie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminopexie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  732. histaminurie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminurie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  733. histaminémie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histaminémie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  734. histidase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  735. histidinase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidinase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  736. histidine --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidine | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  737. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidine-ammoniac-lyase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  738. histidine-décarboxylase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidine-décarboxylase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  739. histidine-désaminase --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=histidine-désaminase | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  740. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=hyperostose vertébrale ankylosante | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  741. hyperoxalurie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=hyperoxalurie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  742. hyperoxalémie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=hyperoxalémie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  743. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  744. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=nystagmus (zone de moindre) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  745. semidominance --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=semidominance | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  746. semiquinone --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=semiquinone | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  747. syndrome de Fuchs --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=syndrome de Fuchs | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  748. séminal --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminal | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  749. séminifère --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminifère | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  750. séminomateux --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminomateux | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  751. séminome --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  752. séminome de l'ovaire --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminome de l'ovaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  753. séminome du médiastin --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminome du médiastin | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  754. séminome spermatocytaire --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=séminome spermatocytaire | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  755. sémiochimique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=sémiochimique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  756. sémiologie extrapyramidale --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=sémiologie extrapyramidale | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  757. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthoastrocytome pléomorphe | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  758. xanthochromie --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthochromie | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  759. xanthochromie caroténique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthochromie caroténique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  760. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthoerythrodermia perstans | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  761. xanthogranulome juvénile --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthogranulome juvénile | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  762. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthogranulome nécrobiotique | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  763. xanthogranulome palpébral --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthogranulome palpébral | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  764. xanthohistiocytome --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthohistiocytome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  765. xanthoma disseminatum --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthoma disseminatum | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
  766. xanthomatose --- r_associated #0: 5 --> en:childhood hypophosphatasia (disorder)
    n1=xanthomatose | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr