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'en:Nathalie syndrome'
(id=16884094 ; fe=en:Nathalie syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=6537 creation date=2021-07-25 touchdate=2025-08-27 16:59:45.000)
≈ 595 relations sortantes

  1. en:Nathalie syndrome -- r_associated #0: 34 / 1 -> syndrome de Nathalie
    n1=en:Nathalie syndrome | n2=syndrome de Nathalie | rel=r_associated | relid=0 | w=34
  2. en:Nathalie syndrome -- r_associated #0: 33 / 0.971 -> syndrome de surdité neurosensorielle-paralysie ponto-bulbaire
    n1=en:Nathalie syndrome | n2=syndrome de surdité neurosensorielle-paralysie ponto-bulbaire | rel=r_associated | relid=0 | w=33
  3. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:adrenal gland hyperplasia ii
    n1=en:Nathalie syndrome | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=30
  4. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:allanson pantzar mcleod syndrome
    n1=en:Nathalie syndrome | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=30
  5. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:alpha-fetoprotein deficiency
    n1=en:Nathalie syndrome | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=30
  6. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:aplasia of lacrimal and salivary glands
    n1=en:Nathalie syndrome | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=30
  7. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:arterial tortuosity syndrome
    n1=en:Nathalie syndrome | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=30
  8. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:auriculo-condylar syndrome
    n1=en:Nathalie syndrome | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=30
  9. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:autosomal dominant hypophosphatemic bone disease
    n1=en:Nathalie syndrome | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=30
  10. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:autosomal recessive asexual dwarfism
    n1=en:Nathalie syndrome | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=30
  11. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:brachymesophalangy 2 and 5
    n1=en:Nathalie syndrome | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=30
  12. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:brown-vialetto-van laere syndrome
    n1=en:Nathalie syndrome | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=30
  13. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:Nathalie syndrome | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=30
  14. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:cervical hydromyelocele
    n1=en:Nathalie syndrome | n2=en:cervical hydromyelocele | rel=r_associated | relid=0 | w=30
  15. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:Nathalie syndrome | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=30
  16. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:cohen syndrome
    n1=en:Nathalie syndrome | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=30
  17. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:congenital anomaly of metacarpal bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of metacarpal bone | rel=r_associated | relid=0 | w=30
  18. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:Nathalie syndrome | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=30
  19. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:crouzon syndrome with acanthosis nigricans (disorder)
    n1=en:Nathalie syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30
  20. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:cutis laxa, autosomal dominant
    n1=en:Nathalie syndrome | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=30
  21. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:deafness-craniofacial syndrome
    n1=en:Nathalie syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=30
  22. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:deficiency of glucosyltransferase 1
    n1=en:Nathalie syndrome | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=30
  23. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:Nathalie syndrome | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=30
  24. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:Nathalie syndrome | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=30
  25. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:Nathalie syndrome | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=30
  26. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:factor v and factor viii, combined deficiency of
    n1=en:Nathalie syndrome | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=30
  27. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:Nathalie syndrome | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30
  28. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:familial interstitial nephritis
    n1=en:Nathalie syndrome | n2=en:familial interstitial nephritis | rel=r_associated | relid=0 | w=30
  29. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:Nathalie syndrome | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=30
  30. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:freeman-sheldon syndrome
    n1=en:Nathalie syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=30
  31. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:glycogen storage disease type i
    n1=en:Nathalie syndrome | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=30
  32. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:hypomagnesemia 1, intestinal
    n1=en:Nathalie syndrome | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=30
  33. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:hypomyelination and congenital cataract
    n1=en:Nathalie syndrome | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=30
  34. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:inherited arthrogryposis
    n1=en:Nathalie syndrome | n2=en:inherited arthrogryposis | rel=r_associated | relid=0 | w=30
  35. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:intestinal epithelial dysplasia
    n1=en:Nathalie syndrome | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=30
  36. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:lecithin acyltransferase deficiency
    n1=en:Nathalie syndrome | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=30
  37. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:lethal congenital contracture syndrome type 3
    n1=en:Nathalie syndrome | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=30
  38. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:macdermot winter syndrome
    n1=en:Nathalie syndrome | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30
  39. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:maple syrup urine disease
    n1=en:Nathalie syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=30
  40. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:marfan syndrome
    n1=en:Nathalie syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=30
  41. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:microcephaly cervical spine fusion anomalies
    n1=en:Nathalie syndrome | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=30
  42. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:Nathalie syndrome | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=30
  43. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:nonaka myopathy
    n1=en:Nathalie syndrome | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=30
  44. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:Nathalie syndrome | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=30
  45. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:oculoskeletal dysplasia
    n1=en:Nathalie syndrome | n2=en:oculoskeletal dysplasia | rel=r_associated | relid=0 | w=30
  46. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:pentosuria
    n1=en:Nathalie syndrome | n2=en:pentosuria | rel=r_associated | relid=0 | w=30
  47. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:pierre robin syndrome with fetal chondrodysplasia
    n1=en:Nathalie syndrome | n2=en:pierre robin syndrome with fetal chondrodysplasia | rel=r_associated | relid=0 | w=30
  48. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:Nathalie syndrome | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=30
  49. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:polyostotic fibrous dysplasia
    n1=en:Nathalie syndrome | n2=en:polyostotic fibrous dysplasia | rel=r_associated | relid=0 | w=30
  50. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:prolonged electroretinal response suppression
    n1=en:Nathalie syndrome | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=30
  51. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:rhizomelic chondrodysplasia punctata
    n1=en:Nathalie syndrome | n2=en:rhizomelic chondrodysplasia punctata | rel=r_associated | relid=0 | w=30
  52. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:rna polymerase iii-related leukodystrophy
    n1=en:Nathalie syndrome | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=30
  53. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:rubella deafness
    n1=en:Nathalie syndrome | n2=en:rubella deafness | rel=r_associated | relid=0 | w=30
  54. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:sly syndrome
    n1=en:Nathalie syndrome | n2=en:sly syndrome | rel=r_associated | relid=0 | w=30
  55. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:spondylocostal dysostosis 4, autosomal dominant
    n1=en:Nathalie syndrome | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=30
  56. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:supernumerary vertebra
    n1=en:Nathalie syndrome | n2=en:supernumerary vertebra | rel=r_associated | relid=0 | w=30
  57. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:tay-sachs disease
    n1=en:Nathalie syndrome | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=30
  58. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:uv-sensitive syndrome
    n1=en:Nathalie syndrome | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=30
  59. en:Nathalie syndrome -- r_associated #0: 30 / 0.882 -> en:wellesley carman french syndrome
    n1=en:Nathalie syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=30
  60. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:Nathalie syndrome | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=29
  61. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:aicardi syndrome
    n1=en:Nathalie syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=29
  62. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:atrophoderma vermiculatum
    n1=en:Nathalie syndrome | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=29
  63. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:autosomal dominant cystoid macular edema
    n1=en:Nathalie syndrome | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=29
  64. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:becker generalized myotonia
    n1=en:Nathalie syndrome | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=29
  65. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:behrens baumann dust syndrome
    n1=en:Nathalie syndrome | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=29
  66. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:benign autosomal dominant osteopetrosis
    n1=en:Nathalie syndrome | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=29
  67. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:cap myopathy
    n1=en:Nathalie syndrome | n2=en:cap myopathy | rel=r_associated | relid=0 | w=29
  68. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:cataract
    n1=en:Nathalie syndrome | n2=en:cataract | rel=r_associated | relid=0 | w=29
  69. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:cataract, congenital, cerulean type 1
    n1=en:Nathalie syndrome | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=29
  70. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:Nathalie syndrome | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=29
  71. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:chondrodysplasia punctata syndrome
    n1=en:Nathalie syndrome | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=29
  72. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:Nathalie syndrome | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=29
  73. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital
    n1=en:Nathalie syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=29
  74. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital anomaly of carpal bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of carpal bone | rel=r_associated | relid=0 | w=29
  75. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital anomaly of lumbar vertebra
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of lumbar vertebra | rel=r_associated | relid=0 | w=29
  76. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital anomaly of radius
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of radius | rel=r_associated | relid=0 | w=29
  77. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital anomaly of rib
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of rib | rel=r_associated | relid=0 | w=29
  78. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital anomaly of thyroid cartilage
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of thyroid cartilage | rel=r_associated | relid=0 | w=29
  79. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital bowing of long bone
    n1=en:Nathalie syndrome | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=29
  80. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
    n1=en:Nathalie syndrome | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=29
  81. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital membranous cataract
    n1=en:Nathalie syndrome | n2=en:congenital membranous cataract | rel=r_associated | relid=0 | w=29
  82. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital pancreatic enterokinase deficiency
    n1=en:Nathalie syndrome | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=29
  83. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital sutural cataract
    n1=en:Nathalie syndrome | n2=en:congenital sutural cataract | rel=r_associated | relid=0 | w=29
  84. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:congenital valgus ankle
    n1=en:Nathalie syndrome | n2=en:congenital valgus ankle | rel=r_associated | relid=0 | w=29
  85. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:cystathionine beta-synthase deficiency disease
    n1=en:Nathalie syndrome | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=29
  86. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:deficiency of fructokinase
    n1=en:Nathalie syndrome | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=29
  87. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:delta phalanx of finger
    n1=en:Nathalie syndrome | n2=en:delta phalanx of finger | rel=r_associated | relid=0 | w=29
  88. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:Nathalie syndrome | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=29
  89. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:Nathalie syndrome | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=29
  90. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:familial renal iminoglycinuria
    n1=en:Nathalie syndrome | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=29
  91. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:femur bifid with monodactylous ectrodactyly
    n1=en:Nathalie syndrome | n2=en:femur bifid with monodactylous ectrodactyly | rel=r_associated | relid=0 | w=29
  92. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:fibrodysplasia ossificans progressiva
    n1=en:Nathalie syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=29
  93. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:Nathalie syndrome | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=29
  94. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:gamma-glutamyltransferase deficiency
    n1=en:Nathalie syndrome | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=29
  95. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:gracile syndrome (disorder)
    n1=en:Nathalie syndrome | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=29
  96. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:hereditary vitreoretinopathy
    n1=en:Nathalie syndrome | n2=en:hereditary vitreoretinopathy | rel=r_associated | relid=0 | w=29
  97. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:histidinemia
    n1=en:Nathalie syndrome | n2=en:histidinemia | rel=r_associated | relid=0 | w=29
  98. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:laurence-moon syndrome
    n1=en:Nathalie syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=29
  99. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:leukotriene c4 synthase deficiency
    n1=en:Nathalie syndrome | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=29
  100. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:majeed syndrome
    n1=en:Nathalie syndrome | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=29
  101. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:maroteaux-lamy syndrome
    n1=en:Nathalie syndrome | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=29
  102. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:Nathalie syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=29
  103. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:microcephaly, amish type (disorder)
    n1=en:Nathalie syndrome | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=29
  104. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:microphthalmia, syndromic 3
    n1=en:Nathalie syndrome | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=29
  105. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis
    n1=en:Nathalie syndrome | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=29
  106. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:myopathy with exercise intolerance, swedish type
    n1=en:Nathalie syndrome | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=29
  107. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:Nathalie syndrome | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=29
  108. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:Nathalie syndrome | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=29
  109. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:orotic aciduria
    n1=en:Nathalie syndrome | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=29
  110. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:papillon-lefevre syndrome
    n1=en:Nathalie syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=29
  111. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:peeling skin syndrome, acral type
    n1=en:Nathalie syndrome | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=29
  112. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:pulmonary interstitial glycogenosis
    n1=en:Nathalie syndrome | n2=en:pulmonary interstitial glycogenosis | rel=r_associated | relid=0 | w=29
  113. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:Nathalie syndrome | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=29
  114. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:radial aplasia-thrombocytopenia syndrome
    n1=en:Nathalie syndrome | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=29
  115. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:sanfilippo syndrome
    n1=en:Nathalie syndrome | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=29
  116. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:sarcosinemia
    n1=en:Nathalie syndrome | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=29
  117. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:schnyder crystalline corneal dystrophy
    n1=en:Nathalie syndrome | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=29
  118. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:smith-mccort dysplasia
    n1=en:Nathalie syndrome | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=29
  119. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:Nathalie syndrome | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=29
  120. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:tetra-amelia autosomal recessive
    n1=en:Nathalie syndrome | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=29
  121. en:Nathalie syndrome -- r_associated #0: 29 / 0.853 -> en:tungland bellman syndrome
    n1=en:Nathalie syndrome | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=29
  122. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:albinotic fundus
    n1=en:Nathalie syndrome | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=28
  123. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:aminomethyltransferase deficiency
    n1=en:Nathalie syndrome | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=28
  124. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:andersen syndrome
    n1=en:Nathalie syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=28
  125. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:Nathalie syndrome | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=28
  126. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:argininemia
    n1=en:Nathalie syndrome | n2=en:argininemia | rel=r_associated | relid=0 | w=28
  127. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:Nathalie syndrome | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=28
  128. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:autosomal dominant pterygium of conjunctiva
    n1=en:Nathalie syndrome | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=28
  129. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:baller-gerold syndrome
    n1=en:Nathalie syndrome | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=28
  130. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:benign congenital myopathy
    n1=en:Nathalie syndrome | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=28
  131. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:brody myopathy
    n1=en:Nathalie syndrome | n2=en:brody myopathy | rel=r_associated | relid=0 | w=28
  132. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:cataract congenital aggravated
    n1=en:Nathalie syndrome | n2=en:cataract congenital aggravated | rel=r_associated | relid=0 | w=28
  133. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:cerebrotendinous xanthomatosis
    n1=en:Nathalie syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=28
  134. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:chronic infantile neurological cutaneous and articular syndrome
    n1=en:Nathalie syndrome | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=28
  135. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts
    n1=en:Nathalie syndrome | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=28
  136. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital anomaly of caudal vertebra
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of caudal vertebra | rel=r_associated | relid=0 | w=28
  137. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital anomaly of humerus
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of humerus | rel=r_associated | relid=0 | w=28
  138. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital anomaly of pelvic bones
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of pelvic bones | rel=r_associated | relid=0 | w=28
  139. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital cataract
    n1=en:Nathalie syndrome | n2=en:congenital cataract | rel=r_associated | relid=0 | w=28
  140. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital combined form cataract
    n1=en:Nathalie syndrome | n2=en:congenital combined form cataract | rel=r_associated | relid=0 | w=28
  141. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital disorder of glycosylation type ia
    n1=en:Nathalie syndrome | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=28
  142. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital leg bone bowing
    n1=en:Nathalie syndrome | n2=en:congenital leg bone bowing | rel=r_associated | relid=0 | w=28
  143. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:Nathalie syndrome | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=28
  144. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:crane-heise syndrome
    n1=en:Nathalie syndrome | n2=en:crane-heise syndrome | rel=r_associated | relid=0 | w=28
  145. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:dubin-johnson syndrome
    n1=en:Nathalie syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=28
  146. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:dysostosis multiplex group
    n1=en:Nathalie syndrome | n2=en:dysostosis multiplex group | rel=r_associated | relid=0 | w=28
  147. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:fronto-facio-nasal dysplasia
    n1=en:Nathalie syndrome | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=28
  148. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:Nathalie syndrome | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=28
  149. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:giacci familial neurogenic acroosteolysis
    n1=en:Nathalie syndrome | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=28
  150. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:hereditary multiple exostoses
    n1=en:Nathalie syndrome | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=28
  151. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=28
  152. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:hyperimmunoglobulin e syndrome
    n1=en:Nathalie syndrome | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=28
  153. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:karandikar maria kamble syndrome
    n1=en:Nathalie syndrome | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=28
  154. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:kuskokwim disease
    n1=en:Nathalie syndrome | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=28
  155. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:Nathalie syndrome | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=28
  156. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:Nathalie syndrome | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=28
  157. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:Nathalie syndrome | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=28
  158. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:microcephaly deafness syndrome
    n1=en:Nathalie syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=28
  159. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:microcephaly-capillary malformation syndrome
    n1=en:Nathalie syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  160. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:microphthalmia, syndromic 4 (disorder)
    n1=en:Nathalie syndrome | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=28
  161. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:mohr-tranebjaerg syndrome
    n1=en:Nathalie syndrome | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=28
  162. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:morquio syndrome
    n1=en:Nathalie syndrome | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=28
  163. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:neonatal progeroid syndrome
    n1=en:Nathalie syndrome | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=28
  164. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:neuroacanthocytosis
    n1=en:Nathalie syndrome | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=28
  165. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:niemann-pick disease
    n1=en:Nathalie syndrome | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=28
  166. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:noise-induced permanent threshold shift
    n1=en:Nathalie syndrome | n2=en:noise-induced permanent threshold shift | rel=r_associated | relid=0 | w=28
  167. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:Nathalie syndrome | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=28
  168. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:pyruvate carboxylase deficiency
    n1=en:Nathalie syndrome | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=28
  169. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:split-hand-foot malformation with long bone deficiency 1
    n1=en:Nathalie syndrome | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=28
  170. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:spondylocamptodactyly
    n1=en:Nathalie syndrome | n2=en:spondylocamptodactyly | rel=r_associated | relid=0 | w=28
  171. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:Nathalie syndrome | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=28
  172. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:stoll levy francfort syndrome
    n1=en:Nathalie syndrome | n2=en:stoll levy francfort syndrome | rel=r_associated | relid=0 | w=28
  173. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:sulfite oxidase deficiency
    n1=en:Nathalie syndrome | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=28
  174. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:thyroid dyshormonogenesis 4
    n1=en:Nathalie syndrome | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=28
  175. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:Nathalie syndrome | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=28
  176. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:transitional lumbosacral vertebra
    n1=en:Nathalie syndrome | n2=en:transitional lumbosacral vertebra | rel=r_associated | relid=0 | w=28
  177. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:tyrosinemia, type iii
    n1=en:Nathalie syndrome | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=28
  178. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:whyte hemingway carpal tarsal phalangeal osteolyses
    n1=en:Nathalie syndrome | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=28
  179. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:x-linked retinal dysplasia
    n1=en:Nathalie syndrome | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=28
  180. en:Nathalie syndrome -- r_associated #0: 28 / 0.824 -> en:xanthinuria, type i
    n1=en:Nathalie syndrome | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=28
  181. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:3-methylglutaconic aciduria type 3
    n1=en:Nathalie syndrome | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=27
  182. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:acid phosphatase deficiency
    n1=en:Nathalie syndrome | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=27
  183. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:acrocallosal syndrome
    n1=en:Nathalie syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=27
  184. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:allgrove syndrome
    n1=en:Nathalie syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=27
  185. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:Nathalie syndrome | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=27
  186. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:Nathalie syndrome | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=27
  187. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:Nathalie syndrome | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=27
  188. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:autosomal recessive ocular albinism
    n1=en:Nathalie syndrome | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=27
  189. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:Nathalie syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=27
  190. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:bothnia retinal dystrophy
    n1=en:Nathalie syndrome | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=27
  191. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:brachydactyly, type a1 (disorder)
    n1=en:Nathalie syndrome | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=27
  192. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:brachyphalangia
    n1=en:Nathalie syndrome | n2=en:brachyphalangia | rel=r_associated | relid=0 | w=27
  193. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:Nathalie syndrome | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=27
  194. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:col1a1 associated connective tissue disorder
    n1=en:Nathalie syndrome | n2=en:col1a1 associated connective tissue disorder | rel=r_associated | relid=0 | w=27
  195. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital ankylosis of elbow
    n1=en:Nathalie syndrome | n2=en:congenital ankylosis of elbow | rel=r_associated | relid=0 | w=27
  196. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital anomaly of lacrimal bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of lacrimal bone | rel=r_associated | relid=0 | w=27
  197. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital anomaly of tarsal bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of tarsal bone | rel=r_associated | relid=0 | w=27
  198. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital anomaly of tibia
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of tibia | rel=r_associated | relid=0 | w=27
  199. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital hereditary muscular dystrophy
    n1=en:Nathalie syndrome | n2=en:congenital hereditary muscular dystrophy | rel=r_associated | relid=0 | w=27
  200. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital hypoplasia of clavicle
    n1=en:Nathalie syndrome | n2=en:congenital hypoplasia of clavicle | rel=r_associated | relid=0 | w=27
  201. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital lamellar cataract
    n1=en:Nathalie syndrome | n2=en:congenital lamellar cataract | rel=r_associated | relid=0 | w=27
  202. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:congenital malformation of sternum
    n1=en:Nathalie syndrome | n2=en:congenital malformation of sternum | rel=r_associated | relid=0 | w=27
  203. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:craniodiaphyseal dysplasia
    n1=en:Nathalie syndrome | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=27
  204. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:cytochrome-c oxidase deficiency
    n1=en:Nathalie syndrome | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=27
  205. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:deafness oligodontia syndrome
    n1=en:Nathalie syndrome | n2=en:deafness oligodontia syndrome | rel=r_associated | relid=0 | w=27
  206. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:ear, patella, short stature syndrome
    n1=en:Nathalie syndrome | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=27
  207. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:Nathalie syndrome | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=27
  208. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:embryonal nuclear cataract (disorder)
    n1=en:Nathalie syndrome | n2=en:embryonal nuclear cataract (disorder) | rel=r_associated | relid=0 | w=27
  209. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:Nathalie syndrome | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=27
  210. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:growth disorders
    n1=en:Nathalie syndrome | n2=en:growth disorders | rel=r_associated | relid=0 | w=27
  211. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:heide syndrome
    n1=en:Nathalie syndrome | n2=en:heide syndrome | rel=r_associated | relid=0 | w=27
  212. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:Nathalie syndrome | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=27
  213. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:Nathalie syndrome | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=27
  214. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:Nathalie syndrome | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=27
  215. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=27
  216. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hnsha due to glutathione reductase deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=27
  217. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hyperferritinemia, hereditary, with congenital cataracts
    n1=en:Nathalie syndrome | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=27
  218. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:Nathalie syndrome | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=27
  219. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:isolated congenital alacrima
    n1=en:Nathalie syndrome | n2=en:isolated congenital alacrima | rel=r_associated | relid=0 | w=27
  220. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:isovaleric acidemia
    n1=en:Nathalie syndrome | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=27
  221. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:lactase deficiency, congenital
    n1=en:Nathalie syndrome | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=27
  222. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:lethal congenital contracture syndrome 1
    n1=en:Nathalie syndrome | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=27
  223. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:Nathalie syndrome | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=27
  224. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:marden-walker syndrome
    n1=en:Nathalie syndrome | n2=en:marden-walker syndrome | rel=r_associated | relid=0 | w=27
  225. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:muscle amp deaminase deficiency
    n1=en:Nathalie syndrome | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=27
  226. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:muscle atrophy
    n1=en:Nathalie syndrome | n2=en:muscle atrophy | rel=r_associated | relid=0 | w=27
  227. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:muscle l-lactate dehydrogenase deficiency
    n1=en:Nathalie syndrome | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  228. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:myopathy, distal, tateyama type
    n1=en:Nathalie syndrome | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=27
  229. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:n-acetylglutamate synthase deficiency
    n1=en:Nathalie syndrome | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=27
  230. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:naxos disease
    n1=en:Nathalie syndrome | n2=en:naxos disease | rel=r_associated | relid=0 | w=27
  231. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:nemaline myopathy 3
    n1=en:Nathalie syndrome | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=27
  232. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:Nathalie syndrome | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=27
  233. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:osteogenesis imperfecta, levin type
    n1=en:Nathalie syndrome | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=27
  234. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts
    n1=en:Nathalie syndrome | n2=en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts | rel=r_associated | relid=0 | w=27
  235. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:pelizaeus merzbacher like disease
    n1=en:Nathalie syndrome | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=27
  236. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:peters-plus syndrome
    n1=en:Nathalie syndrome | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=27
  237. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:phenylketonuria ii
    n1=en:Nathalie syndrome | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=27
  238. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:pseudocholinesterase deficiency
    n1=en:Nathalie syndrome | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=27
  239. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:pseudotrisomy 13 syndrome
    n1=en:Nathalie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  240. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:rapadilino syndrome
    n1=en:Nathalie syndrome | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=27
  241. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:Nathalie syndrome | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=27
  242. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:sitosterolemia with xanthomatosis
    n1=en:Nathalie syndrome | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=27
  243. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:Nathalie syndrome | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=27
  244. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:Nathalie syndrome | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=27
  245. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:tarsal-carpal coalition syndrome
    n1=en:Nathalie syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=27
  246. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:thomas syndrome
    n1=en:Nathalie syndrome | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=27
  247. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:trichohepatoenteric syndrome
    n1=en:Nathalie syndrome | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=27
  248. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:trichorhinophalangeal syndrome type ii
    n1=en:Nathalie syndrome | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=27
  249. en:Nathalie syndrome -- r_associated #0: 27 / 0.794 -> en:wolman disease
    n1=en:Nathalie syndrome | n2=en:wolman disease | rel=r_associated | relid=0 | w=27
  250. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:Nathalie syndrome | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=26
  251. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:acrodysostosis
    n1=en:Nathalie syndrome | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=26
  252. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:albinism, ocular
    n1=en:Nathalie syndrome | n2=en:albinism, ocular | rel=r_associated | relid=0 | w=26
  253. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:aminoacylase 1 deficiency
    n1=en:Nathalie syndrome | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=26
  254. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:autosomal recessive primary microcephaly
    n1=en:Nathalie syndrome | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=26
  255. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:avascular necrosis of femoral head
    n1=en:Nathalie syndrome | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=26
  256. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:bardet-biedl syndrome
    n1=en:Nathalie syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=26
  257. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:bifid patella
    n1=en:Nathalie syndrome | n2=en:bifid patella | rel=r_associated | relid=0 | w=26
  258. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:cerebellar ataxia, cayman type
    n1=en:Nathalie syndrome | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=26
  259. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:Nathalie syndrome | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=26
  260. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:charcot-marie-tooth disease type 4
    n1=en:Nathalie syndrome | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=26
  261. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:charcot-marie-tooth disease, demyelinating, type 1e
    n1=en:Nathalie syndrome | n2=en:charcot-marie-tooth disease, demyelinating, type 1e | rel=r_associated | relid=0 | w=26
  262. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:chondrodysplasia
    n1=en:Nathalie syndrome | n2=en:chondrodysplasia | rel=r_associated | relid=0 | w=26
  263. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:citrin deficiency
    n1=en:Nathalie syndrome | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=26
  264. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:Nathalie syndrome | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=26
  265. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:congenital anomaly of sternebra
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of sternebra | rel=r_associated | relid=0 | w=26
  266. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:congenital disorder of glycosylation type ig
    n1=en:Nathalie syndrome | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=26
  267. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:congenital sucrase-isomaltase deficiency
    n1=en:Nathalie syndrome | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=26
  268. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:congenital transferrin deficiency
    n1=en:Nathalie syndrome | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=26
  269. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:cryptophthalmos syndrome
    n1=en:Nathalie syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=26
  270. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:cutis laxa, autosomal recessive
    n1=en:Nathalie syndrome | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=26
  271. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:desmosterolosis
    n1=en:Nathalie syndrome | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=26
  272. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:dicarboxylicaminoaciduria
    n1=en:Nathalie syndrome | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=26
  273. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:familial digital arthropathy and brachydactyly syndrome
    n1=en:Nathalie syndrome | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=26
  274. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:familial osteochondritis dissecans
    n1=en:Nathalie syndrome | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=26
  275. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:farber lipogranulomatosis
    n1=en:Nathalie syndrome | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=26
  276. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:glutamate formiminotransferase deficiency
    n1=en:Nathalie syndrome | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=26
  277. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:hereditary factor xi deficiency disease
    n1=en:Nathalie syndrome | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=26
  278. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:Nathalie syndrome | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=26
  279. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:hmg-coa lyase deficiency
    n1=en:Nathalie syndrome | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=26
  280. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:hnsha due to aldolase a deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=26
  281. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=26
  282. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:klippel-feil syndrome
    n1=en:Nathalie syndrome | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=26
  283. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:Nathalie syndrome | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=26
  284. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:Nathalie syndrome | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=26
  285. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:microphthalmia, syndromic 1
    n1=en:Nathalie syndrome | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=26
  286. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:non-dystrophic myotonia
    n1=en:Nathalie syndrome | n2=en:non-dystrophic myotonia | rel=r_associated | relid=0 | w=26
  287. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:north american indian childhood cirrhosis
    n1=en:Nathalie syndrome | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=26
  288. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:pontocerebellar hypoplasia type 2
    n1=en:Nathalie syndrome | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=26
  289. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:Nathalie syndrome | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=26
  290. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:prolidase deficiency
    n1=en:Nathalie syndrome | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=26
  291. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:prune belly syndrome
    n1=en:Nathalie syndrome | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=26
  292. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:robinow syndrome
    n1=en:Nathalie syndrome | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=26
  293. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:shwachman-diamond syndrome
    n1=en:Nathalie syndrome | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=26
  294. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:skeletal dysplasia
    n1=en:Nathalie syndrome | n2=en:skeletal dysplasia | rel=r_associated | relid=0 | w=26
  295. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:Nathalie syndrome | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=26
  296. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:spondyloepiphyseal dysplasia tarda, x-linked
    n1=en:Nathalie syndrome | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=26
  297. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:stickler syndrome
    n1=en:Nathalie syndrome | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=26
  298. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:Nathalie syndrome | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=26
  299. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:type ii acrocephalopolysyndactyly
    n1=en:Nathalie syndrome | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=26
  300. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:tyrosinemia type ii
    n1=en:Nathalie syndrome | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=26
  301. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:valinemia
    n1=en:Nathalie syndrome | n2=en:valinemia | rel=r_associated | relid=0 | w=26
  302. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:walker-warburg syndrome
    n1=en:Nathalie syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=26
  303. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> en:warsaw breakage syndrome
    n1=en:Nathalie syndrome | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=26
  304. en:Nathalie syndrome -- r_associated #0: 26 / 0.765 -> Nathalie
    n1=en:Nathalie syndrome | n2=Nathalie | rel=r_associated | relid=0 | w=26
  305. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:acrodermatitis enteropathica
    n1=en:Nathalie syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=25
  306. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:alkaptonuria
    n1=en:Nathalie syndrome | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=25
  307. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:ataxia telangiectasia syndrome
    n1=en:Nathalie syndrome | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=25
  308. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:ateliotic dwarfism without insulinopenia
    n1=en:Nathalie syndrome | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=25
  309. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:autosomal recessive ichthyosis
    n1=en:Nathalie syndrome | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=25
  310. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:behr syndrome
    n1=en:Nathalie syndrome | n2=en:behr syndrome | rel=r_associated | relid=0 | w=25
  311. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:brachydactyly syndrome type b
    n1=en:Nathalie syndrome | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=25
  312. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital abnormal shape of clavicle
    n1=en:Nathalie syndrome | n2=en:congenital abnormal shape of clavicle | rel=r_associated | relid=0 | w=25
  313. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital anomaly of bone and joint
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of bone and joint | rel=r_associated | relid=0 | w=25
  314. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital anomaly of fetal head bones
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of fetal head bones | rel=r_associated | relid=0 | w=25
  315. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital anomaly of hyoid bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of hyoid bone | rel=r_associated | relid=0 | w=25
  316. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital cataract and lens anomalies
    n1=en:Nathalie syndrome | n2=en:congenital cataract and lens anomalies | rel=r_associated | relid=0 | w=25
  317. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital disorder of glycosylation type ic
    n1=en:Nathalie syndrome | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=25
  318. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital dyserythropoietic anemia, type i
    n1=en:Nathalie syndrome | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=25
  319. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital fusion of spine
    n1=en:Nathalie syndrome | n2=en:congenital fusion of spine | rel=r_associated | relid=0 | w=25
  320. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital polar cataract
    n1=en:Nathalie syndrome | n2=en:congenital polar cataract | rel=r_associated | relid=0 | w=25
  321. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:congenital subtotal cataract
    n1=en:Nathalie syndrome | n2=en:congenital subtotal cataract | rel=r_associated | relid=0 | w=25
  322. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:cortical and zonular cataract
    n1=en:Nathalie syndrome | n2=en:cortical and zonular cataract | rel=r_associated | relid=0 | w=25
  323. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:cystinosis
    n1=en:Nathalie syndrome | n2=en:cystinosis | rel=r_associated | relid=0 | w=25
  324. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:distal arthrogryposis syndrome
    n1=en:Nathalie syndrome | n2=en:distal arthrogryposis syndrome | rel=r_associated | relid=0 | w=25
  325. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:duplication of lower limb bone
    n1=en:Nathalie syndrome | n2=en:duplication of lower limb bone | rel=r_associated | relid=0 | w=25
  326. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:ehlers-danlos syndrome
    n1=en:Nathalie syndrome | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=25
  327. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:Nathalie syndrome | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=25
  328. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:glycogen storage disease 0, liver
    n1=en:Nathalie syndrome | n2=en:glycogen storage disease 0, liver | rel=r_associated | relid=0 | w=25
  329. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:hepatolenticular degeneration
    n1=en:Nathalie syndrome | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=25
  330. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:Nathalie syndrome | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=25
  331. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:hereditary factor xii deficiency disease
    n1=en:Nathalie syndrome | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=25
  332. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:hydromeningocele
    n1=en:Nathalie syndrome | n2=en:hydromeningocele | rel=r_associated | relid=0 | w=25
  333. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:Nathalie syndrome | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=25
  334. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:isolated hyperchlorhidrosis
    n1=en:Nathalie syndrome | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=25
  335. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:joubert syndrome
    n1=en:Nathalie syndrome | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=25
  336. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:klippel-trenaunay-weber syndrome
    n1=en:Nathalie syndrome | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=25
  337. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:lipoprotein glomerulopathy
    n1=en:Nathalie syndrome | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=25
  338. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:Nathalie syndrome | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=25
  339. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:multiple sulfatase deficiency disease
    n1=en:Nathalie syndrome | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=25
  340. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:neuraminidase deficiency
    n1=en:Nathalie syndrome | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=25
  341. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:noise-induced temporary threshold shift
    n1=en:Nathalie syndrome | n2=en:noise-induced temporary threshold shift | rel=r_associated | relid=0 | w=25
  342. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:nonnuclear polymorphic congenital cataract
    n1=en:Nathalie syndrome | n2=en:nonnuclear polymorphic congenital cataract | rel=r_associated | relid=0 | w=25
  343. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:Nathalie syndrome | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=25
  344. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:potassium aggravated myotonia
    n1=en:Nathalie syndrome | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=25
  345. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:Nathalie syndrome | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=25
  346. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:propionic acidemia
    n1=en:Nathalie syndrome | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=25
  347. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:sonoda syndrome
    n1=en:Nathalie syndrome | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=25
  348. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:Nathalie syndrome | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=25
  349. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:spondyloenchondrodysplasia
    n1=en:Nathalie syndrome | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=25
  350. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:Nathalie syndrome | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=25
  351. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:triglyceride storage disease with ichthyosis
    n1=en:Nathalie syndrome | n2=en:triglyceride storage disease with ichthyosis | rel=r_associated | relid=0 | w=25
  352. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:wells jankovic syndrome
    n1=en:Nathalie syndrome | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=25
  353. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
    n1=en:Nathalie syndrome | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=25
  354. en:Nathalie syndrome -- r_associated #0: 25 / 0.735 -> Nathalie (syndrome de)
    n1=en:Nathalie syndrome | n2=Nathalie (syndrome de) | rel=r_associated | relid=0 | w=25
  355. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:21-hydroxylase deficiency
    n1=en:Nathalie syndrome | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=24
  356. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:3-methylglutaconic aciduria type 1
    n1=en:Nathalie syndrome | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=24
  357. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:3-methylglutaconic aciduria type iv
    n1=en:Nathalie syndrome | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=24
  358. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:Nathalie syndrome | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=24
  359. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:accessory ossification center
    n1=en:Nathalie syndrome | n2=en:accessory ossification center | rel=r_associated | relid=0 | w=24
  360. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:alpha-1 antitrypsin deficiency
    n1=en:Nathalie syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=24
  361. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:Nathalie syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=24
  362. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:argininosuccinic aciduria
    n1=en:Nathalie syndrome | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=24
  363. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:ataxia with vitamin e deficiency
    n1=en:Nathalie syndrome | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=24
  364. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:atelosteogenesis, type 1
    n1=en:Nathalie syndrome | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=24
  365. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:autosomal recessive scid
    n1=en:Nathalie syndrome | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=24
  366. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:Nathalie syndrome | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=24
  367. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:bads syndrome
    n1=en:Nathalie syndrome | n2=en:bads syndrome | rel=r_associated | relid=0 | w=24
  368. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:Nathalie syndrome | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=24
  369. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:bowen-conradi syndrome
    n1=en:Nathalie syndrome | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=24
  370. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:centronuclear myopathy 1
    n1=en:Nathalie syndrome | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=24
  371. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:clavicle, pseudarthrosis of, congenital
    n1=en:Nathalie syndrome | n2=en:clavicle, pseudarthrosis of, congenital | rel=r_associated | relid=0 | w=24
  372. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:congenital absence of skeletal bone
    n1=en:Nathalie syndrome | n2=en:congenital absence of skeletal bone | rel=r_associated | relid=0 | w=24
  373. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:congenital anomaly of thoracic vertebra
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of thoracic vertebra | rel=r_associated | relid=0 | w=24
  374. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:congenital leptin deficiency
    n1=en:Nathalie syndrome | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=24
  375. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:congenital subcapsular cataract
    n1=en:Nathalie syndrome | n2=en:congenital subcapsular cataract | rel=r_associated | relid=0 | w=24
  376. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:congenital varus ankle
    n1=en:Nathalie syndrome | n2=en:congenital varus ankle | rel=r_associated | relid=0 | w=24
  377. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:deafness
    n1=en:Nathalie syndrome | n2=en:deafness | rel=r_associated | relid=0 | w=24
  378. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:deafness, sensorineural, and male infertility
    n1=en:Nathalie syndrome | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=24
  379. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:failure of differentiation of bones of forearm
    n1=en:Nathalie syndrome | n2=en:failure of differentiation of bones of forearm | rel=r_associated | relid=0 | w=24
  380. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:familial arthrogryposis-cholestatic hepatorenal syndrome
    n1=en:Nathalie syndrome | n2=en:familial arthrogryposis-cholestatic hepatorenal syndrome | rel=r_associated | relid=0 | w=24
  381. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:fucosidosis
    n1=en:Nathalie syndrome | n2=en:fucosidosis | rel=r_associated | relid=0 | w=24
  382. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:genetic disorder
    n1=en:Nathalie syndrome | n2=en:genetic disorder | rel=r_associated | relid=0 | w=24
  383. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:geroderma osteodysplastica
    n1=en:Nathalie syndrome | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=24
  384. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:glutathione synthetase deficiency
    n1=en:Nathalie syndrome | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=24
  385. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:hereditary tubulointerstitial disorder
    n1=en:Nathalie syndrome | n2=en:hereditary tubulointerstitial disorder | rel=r_associated | relid=0 | w=24
  386. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:hypermobility syndrome
    n1=en:Nathalie syndrome | n2=en:hypermobility syndrome | rel=r_associated | relid=0 | w=24
  387. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:i-cell disease
    n1=en:Nathalie syndrome | n2=en:i-cell disease | rel=r_associated | relid=0 | w=24
  388. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:infantile hypophosphatasia
    n1=en:Nathalie syndrome | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=24
  389. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:jackson-weiss syndrome
    n1=en:Nathalie syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=24
  390. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:jervell and lange nielsen syndrome
    n1=en:Nathalie syndrome | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=24
  391. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:keratitis, hereditary
    n1=en:Nathalie syndrome | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=24
  392. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:knuckle pads, leuconychia and sensorineural deafness
    n1=en:Nathalie syndrome | n2=en:knuckle pads, leuconychia and sensorineural deafness | rel=r_associated | relid=0 | w=24
  393. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:lack of ossification of clavicle
    n1=en:Nathalie syndrome | n2=en:lack of ossification of clavicle | rel=r_associated | relid=0 | w=24
  394. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:longitudinal deficiency of femur
    n1=en:Nathalie syndrome | n2=en:longitudinal deficiency of femur | rel=r_associated | relid=0 | w=24
  395. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:Nathalie syndrome | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=24
  396. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:microcephalic primordial dwarfism toriello type
    n1=en:Nathalie syndrome | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=24
  397. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:microcornea with glaucoma and absent frontal sinus syndrome
    n1=en:Nathalie syndrome | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=24
  398. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:Nathalie syndrome | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=24
  399. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:Nathalie syndrome | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=24
  400. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:myopathy with abnormal lipid metabolism
    n1=en:Nathalie syndrome | n2=en:myopathy with abnormal lipid metabolism | rel=r_associated | relid=0 | w=24
  401. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:nance-horan syndrome
    n1=en:Nathalie syndrome | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=24
  402. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:northern epilepsy syndrome
    n1=en:Nathalie syndrome | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=24
  403. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:odontohypophosphatasia (disorder)
    n1=en:Nathalie syndrome | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=24
  404. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:okihiro syndrome
    n1=en:Nathalie syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=24
  405. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:osteopetrosis
    n1=en:Nathalie syndrome | n2=en:osteopetrosis | rel=r_associated | relid=0 | w=24
  406. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:otoonychoperoneal syndrome
    n1=en:Nathalie syndrome | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=24
  407. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:parietal foramina
    n1=en:Nathalie syndrome | n2=en:parietal foramina | rel=r_associated | relid=0 | w=24
  408. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:primary hyperoxaluria
    n1=en:Nathalie syndrome | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=24
  409. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:pyle metaphyseal dysplasia
    n1=en:Nathalie syndrome | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=24
  410. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias
    n1=en:Nathalie syndrome | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=24
  411. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:reardon hall slaney syndrome
    n1=en:Nathalie syndrome | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=24
  412. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:sellars beighton syndrome
    n1=en:Nathalie syndrome | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=24
  413. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:Nathalie syndrome | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=24
  414. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:thong douglas ferrante syndrome
    n1=en:Nathalie syndrome | n2=en:thong douglas ferrante syndrome | rel=r_associated | relid=0 | w=24
  415. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:total and subtotal congenital cataract
    n1=en:Nathalie syndrome | n2=en:total and subtotal congenital cataract | rel=r_associated | relid=0 | w=24
  416. en:Nathalie syndrome -- r_associated #0: 24 / 0.706 -> en:treacher collins syndrome
    n1=en:Nathalie syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=24
  417. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:al awadi syndrome
    n1=en:Nathalie syndrome | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=23
  418. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:Nathalie syndrome | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=23
  419. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:anomaly of cricoid cartilage
    n1=en:Nathalie syndrome | n2=en:anomaly of cricoid cartilage | rel=r_associated | relid=0 | w=23
  420. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:Nathalie syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=23
  421. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:autosomal dominant epidermolysis bullosa simplex
    n1=en:Nathalie syndrome | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=23
  422. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:Nathalie syndrome | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=23
  423. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:childhood hypophosphatasia (disorder)
    n1=en:Nathalie syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=23
  424. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:classical phenylketonuria
    n1=en:Nathalie syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23
  425. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:cleidocranial dysplasia
    n1=en:Nathalie syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=23
  426. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:combined malonic and methylmalonic aciduria
    n1=en:Nathalie syndrome | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=23
  427. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:congenital anomaly of ulna
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of ulna | rel=r_associated | relid=0 | w=23
  428. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:congenital capsular cataract
    n1=en:Nathalie syndrome | n2=en:congenital capsular cataract | rel=r_associated | relid=0 | w=23
  429. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:congenital unilateral cataract
    n1=en:Nathalie syndrome | n2=en:congenital unilateral cataract | rel=r_associated | relid=0 | w=23
  430. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:corneal dystrophy, congenital stromal
    n1=en:Nathalie syndrome | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=23
  431. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:cystinosis, infantile nephropathic
    n1=en:Nathalie syndrome | n2=en:cystinosis, infantile nephropathic | rel=r_associated | relid=0 | w=23
  432. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:deafness, progressive, with stapes fixation
    n1=en:Nathalie syndrome | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=23
  433. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:Nathalie syndrome | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=23
  434. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:dystrophia myotonica 2
    n1=en:Nathalie syndrome | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=23
  435. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:Nathalie syndrome | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=23
  436. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:ehlers-danlos syndrome, type vi
    n1=en:Nathalie syndrome | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=23
  437. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:familial acantholysis
    n1=en:Nathalie syndrome | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=23
  438. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:familial amyloid polyneuropathy, type v
    n1=en:Nathalie syndrome | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=23
  439. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:familial partial lipodystrophy, type 2
    n1=en:Nathalie syndrome | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=23
  440. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:Nathalie syndrome | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=23
  441. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:gurrieri sammito bellussi syndrome
    n1=en:Nathalie syndrome | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=23
  442. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hanhart's syndrome
    n1=en:Nathalie syndrome | n2=en:hanhart's syndrome | rel=r_associated | relid=0 | w=23
  443. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hereditary choroidal dystrophy
    n1=en:Nathalie syndrome | n2=en:hereditary choroidal dystrophy | rel=r_associated | relid=0 | w=23
  444. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hereditary corneal dystrophy
    n1=en:Nathalie syndrome | n2=en:hereditary corneal dystrophy | rel=r_associated | relid=0 | w=23
  445. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hereditary factor x deficiency disease
    n1=en:Nathalie syndrome | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=23
  446. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hereditary optic atrophy
    n1=en:Nathalie syndrome | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=23
  447. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:Nathalie syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23
  448. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hyperphosphatasia with mental retardation
    n1=en:Nathalie syndrome | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=23
  449. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hyperprolinemia type 2
    n1=en:Nathalie syndrome | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=23
  450. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hypokalemia, familial
    n1=en:Nathalie syndrome | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=23
  451. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:hypoplastic tibia and postaxial polydactyly syndrome
    n1=en:Nathalie syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=23
  452. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1
    n1=en:Nathalie syndrome | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=23
  453. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:isaacs syndrome
    n1=en:Nathalie syndrome | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=23
  454. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:jankovic rivera syndrome
    n1=en:Nathalie syndrome | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=23
  455. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:macular corneal dystrophy
    n1=en:Nathalie syndrome | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=23
  456. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:Nathalie syndrome | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=23
  457. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:metaphyseal dysplasia, braun-tinschert type
    n1=en:Nathalie syndrome | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=23
  458. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:Nathalie syndrome | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=23
  459. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:nail-patella syndrome
    n1=en:Nathalie syndrome | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=23
  460. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:netherton syndrome
    n1=en:Nathalie syndrome | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=23
  461. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:oculocutaneous albinism
    n1=en:Nathalie syndrome | n2=en:oculocutaneous albinism | rel=r_associated | relid=0 | w=23
  462. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:other congenital cataract and lens anomalies
    n1=en:Nathalie syndrome | n2=en:other congenital cataract and lens anomalies | rel=r_associated | relid=0 | w=23
  463. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:presentey anomaly
    n1=en:Nathalie syndrome | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=23
  464. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:Nathalie syndrome | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=23
  465. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:Nathalie syndrome | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=23
  466. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:Nathalie syndrome | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=23
  467. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:retinitis punctata albescens (disorder)
    n1=en:Nathalie syndrome | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=23
  468. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:rubella cataract
    n1=en:Nathalie syndrome | n2=en:rubella cataract | rel=r_associated | relid=0 | w=23
  469. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:Nathalie syndrome | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=23
  470. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:spinocerebellar ataxia with epilepsy
    n1=en:Nathalie syndrome | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=23
  471. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:spondylo-ocular syndrome
    n1=en:Nathalie syndrome | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=23
  472. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:Nathalie syndrome | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=23
  473. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:syndrome, branchio-oculo-facial
    n1=en:Nathalie syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=23
  474. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:ulna metaphyseal dysplasia syndrome
    n1=en:Nathalie syndrome | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=23
  475. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:Nathalie syndrome | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=23
  476. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:urocanase deficiency
    n1=en:Nathalie syndrome | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=23
  477. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> en:zellweger syndrome
    n1=en:Nathalie syndrome | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=23
  478. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> syndrome
    n1=en:Nathalie syndrome | n2=syndrome | rel=r_associated | relid=0 | w=23
  479. en:Nathalie syndrome -- r_associated #0: 23 / 0.676 -> syndrome de
    n1=en:Nathalie syndrome | n2=syndrome de | rel=r_associated | relid=0 | w=23
  480. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:2-hydroxyglutaric aciduria
    n1=en:Nathalie syndrome | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=22
  481. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:3-methylglutaconic aciduria type 5
    n1=en:Nathalie syndrome | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=22
  482. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:absence deformity of leg and congenital cataract syndrome
    n1=en:Nathalie syndrome | n2=en:absence deformity of leg and congenital cataract syndrome | rel=r_associated | relid=0 | w=22
  483. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:acromicric dysplasia
    n1=en:Nathalie syndrome | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=22
  484. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:alpha, alpha-trehalase deficiency
    n1=en:Nathalie syndrome | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=22
  485. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:alstrom syndrome
    n1=en:Nathalie syndrome | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=22
  486. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:Nathalie syndrome | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=22
  487. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:aspartylglycosaminuria
    n1=en:Nathalie syndrome | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=22
  488. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:autosomal recessive sideroblastic anemia
    n1=en:Nathalie syndrome | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=22
  489. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:brachydactyly type a6
    n1=en:Nathalie syndrome | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=22
  490. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:closed spina bifida with arnold-chiari malformation
    n1=en:Nathalie syndrome | n2=en:closed spina bifida with arnold-chiari malformation | rel=r_associated | relid=0 | w=22
  491. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital adrenal hyperplasia
    n1=en:Nathalie syndrome | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=22
  492. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:Nathalie syndrome | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=22
  493. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital anomaly of cervical vertebra
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of cervical vertebra | rel=r_associated | relid=0 | w=22
  494. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital anomaly of femur
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of femur | rel=r_associated | relid=0 | w=22
  495. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital anomaly of metatarsal bone
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of metatarsal bone | rel=r_associated | relid=0 | w=22
  496. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital anomaly of vomer
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of vomer | rel=r_associated | relid=0 | w=22
  497. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital capsular and subcapsular cataract
    n1=en:Nathalie syndrome | n2=en:congenital capsular and subcapsular cataract | rel=r_associated | relid=0 | w=22
  498. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:Nathalie syndrome | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=22
  499. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital laryngomalacia
    n1=en:Nathalie syndrome | n2=en:congenital laryngomalacia | rel=r_associated | relid=0 | w=22
  500. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital thickening of clavicle
    n1=en:Nathalie syndrome | n2=en:congenital thickening of clavicle | rel=r_associated | relid=0 | w=22
  501. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:congenital total cataract
    n1=en:Nathalie syndrome | n2=en:congenital total cataract | rel=r_associated | relid=0 | w=22
  502. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:corpus callosum agenesis neuronopathy
    n1=en:Nathalie syndrome | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=22
  503. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:Nathalie syndrome | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=22
  504. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:dermoids of cornea
    n1=en:Nathalie syndrome | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=22
  505. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:donnai-barrow syndrome
    n1=en:Nathalie syndrome | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=22
  506. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:ectromelia
    n1=en:Nathalie syndrome | n2=en:ectromelia | rel=r_associated | relid=0 | w=22
  507. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:enterokinase deficiency
    n1=en:Nathalie syndrome | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=22
  508. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:familial hypoaldosteronism
    n1=en:Nathalie syndrome | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=22
  509. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:Nathalie syndrome | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=22
  510. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:fleck corneal dystrophy
    n1=en:Nathalie syndrome | n2=en:fleck corneal dystrophy | rel=r_associated | relid=0 | w=22
  511. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:glycogen storage disease type x
    n1=en:Nathalie syndrome | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=22
  512. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:glycogen storage disease, muscular form
    n1=en:Nathalie syndrome | n2=en:glycogen storage disease, muscular form | rel=r_associated | relid=0 | w=22
  513. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:Nathalie syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=22
  514. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:Nathalie syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=22
  515. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:hemivertebra
    n1=en:Nathalie syndrome | n2=en:hemivertebra | rel=r_associated | relid=0 | w=22
  516. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:hereditary fructose intolerance
    n1=en:Nathalie syndrome | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=22
  517. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:hereditary myopathy with early respiratory failure
    n1=en:Nathalie syndrome | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=22
  518. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:Nathalie syndrome | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=22
  519. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:incomplete ossification of clavicle
    n1=en:Nathalie syndrome | n2=en:incomplete ossification of clavicle | rel=r_associated | relid=0 | w=22
  520. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:kaufman-mckusick syndrome
    n1=en:Nathalie syndrome | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=22
  521. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:laron syndrome
    n1=en:Nathalie syndrome | n2=en:laron syndrome | rel=r_associated | relid=0 | w=22
  522. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:Nathalie syndrome | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=22
  523. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:longitudinal deficiency of tibia and/or fibula
    n1=en:Nathalie syndrome | n2=en:longitudinal deficiency of tibia and/or fibula | rel=r_associated | relid=0 | w=22
  524. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:lowry yong syndrome
    n1=en:Nathalie syndrome | n2=en:lowry yong syndrome | rel=r_associated | relid=0 | w=22
  525. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:mannosidosis
    n1=en:Nathalie syndrome | n2=en:mannosidosis | rel=r_associated | relid=0 | w=22
  526. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:marles greenberg persaud syndrome
    n1=en:Nathalie syndrome | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=22
  527. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:Nathalie syndrome | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=22
  528. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:microcornea with corectopia and macular hypoplasia syndrome
    n1=en:Nathalie syndrome | n2=en:microcornea with corectopia and macular hypoplasia syndrome | rel=r_associated | relid=0 | w=22
  529. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:Nathalie syndrome | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=22
  530. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:mucopolysaccharidosis type i
    n1=en:Nathalie syndrome | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=22
  531. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:muscular dystrophy, oculopharyngeal
    n1=en:Nathalie syndrome | n2=en:muscular dystrophy, oculopharyngeal | rel=r_associated | relid=0 | w=22
  532. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:neutral lipid storage disease with myopathy
    n1=en:Nathalie syndrome | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=22
  533. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:oculocutaneous albinism type 4
    n1=en:Nathalie syndrome | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=22
  534. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:osteochondritis
    n1=en:Nathalie syndrome | n2=en:osteochondritis | rel=r_associated | relid=0 | w=22
  535. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:persistent mullerian duct syndrome
    n1=en:Nathalie syndrome | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=22
  536. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:porphobilinogen synthase deficiency
    n1=en:Nathalie syndrome | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=22
  537. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:primary hypertrophic osteoarthropathy
    n1=en:Nathalie syndrome | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=22
  538. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:saito kuba tsuruta syndrome
    n1=en:Nathalie syndrome | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=22
  539. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:severe early childhood onset retinal dystrophy
    n1=en:Nathalie syndrome | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=22
  540. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:spondylocostal dysostosis
    n1=en:Nathalie syndrome | n2=en:spondylocostal dysostosis | rel=r_associated | relid=0 | w=22
  541. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:Nathalie syndrome | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=22
  542. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:transcobalamin ii deficiency
    n1=en:Nathalie syndrome | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=22
  543. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:type i acrocephalosyndactyly
    n1=en:Nathalie syndrome | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=22
  544. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:type v acrocephalosyndactyly
    n1=en:Nathalie syndrome | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=22
  545. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:waardenburg anophthalmia syndrome
    n1=en:Nathalie syndrome | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=22
  546. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:werdnig-hoffmann disease
    n1=en:Nathalie syndrome | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=22
  547. en:Nathalie syndrome -- r_associated #0: 22 / 0.647 -> en:xeroderma pigmentosum
    n1=en:Nathalie syndrome | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=22
  548. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:5-oxoprolinase deficiency
    n1=en:Nathalie syndrome | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=21
  549. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:Nathalie syndrome | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=21
  550. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:Nathalie syndrome | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=21
  551. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:Nathalie syndrome | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=21
  552. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:Nathalie syndrome | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=21
  553. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:basal ganglia disease, biotin-responsive
    n1=en:Nathalie syndrome | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=21
  554. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:beta-aminoisobutyricaciduria
    n1=en:Nathalie syndrome | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=21
  555. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:biotinidase deficiency
    n1=en:Nathalie syndrome | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=21
  556. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:brachyolmia type 3
    n1=en:Nathalie syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=21
  557. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:brittle cornea syndrome 1
    n1=en:Nathalie syndrome | n2=en:brittle cornea syndrome 1 | rel=r_associated | relid=0 | w=21
  558. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:chitty hall baraitser syndrome
    n1=en:Nathalie syndrome | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=21
  559. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:chylomicron retention disease
    n1=en:Nathalie syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=21
  560. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital abnormality
    n1=en:Nathalie syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=21
  561. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital abnormality of skull and face bones
    n1=en:Nathalie syndrome | n2=en:congenital abnormality of skull and face bones | rel=r_associated | relid=0 | w=21
  562. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital anomaly of fibula
    n1=en:Nathalie syndrome | n2=en:congenital anomaly of fibula | rel=r_associated | relid=0 | w=21
  563. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital bilateral cataracts
    n1=en:Nathalie syndrome | n2=en:congenital bilateral cataracts | rel=r_associated | relid=0 | w=21
  564. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital bony fusion of phalanges
    n1=en:Nathalie syndrome | n2=en:congenital bony fusion of phalanges | rel=r_associated | relid=0 | w=21
  565. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital cortical cataract
    n1=en:Nathalie syndrome | n2=en:congenital cortical cataract | rel=r_associated | relid=0 | w=21
  566. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital deformity of scapula
    n1=en:Nathalie syndrome | n2=en:congenital deformity of scapula | rel=r_associated | relid=0 | w=21
  567. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:Nathalie syndrome | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=21
  568. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:congenital synostosis of lower limb bones
    n1=en:Nathalie syndrome | n2=en:congenital synostosis of lower limb bones | rel=r_associated | relid=0 | w=21
  569. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:crigler-najjar syndrome
    n1=en:Nathalie syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=21
  570. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:crisponi syndrome
    n1=en:Nathalie syndrome | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=21
  571. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:dysplasia, saddan
    n1=en:Nathalie syndrome | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=21
  572. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:ethanolaminosis
    n1=en:Nathalie syndrome | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=21
  573. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:fryns macrocephaly
    n1=en:Nathalie syndrome | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=21
  574. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:generalized myotonia of thomsen
    n1=en:Nathalie syndrome | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=21
  575. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:glutamate-cysteine ligase deficiency
    n1=en:Nathalie syndrome | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=21
  576. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:hereditary retinal dystrophy
    n1=en:Nathalie syndrome | n2=en:hereditary retinal dystrophy | rel=r_associated | relid=0 | w=21
  577. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:Nathalie syndrome | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=21
  578. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:hyperprolinemia type 1
    n1=en:Nathalie syndrome | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=21
  579. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:hypospadias-mental retardation syndrome
    n1=en:Nathalie syndrome | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=21
  580. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:infantile globoid cell leukodystrophy
    n1=en:Nathalie syndrome | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=21
  581. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:isolated hypoplasia of the right ventricle
    n1=en:Nathalie syndrome | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=21
  582. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:joubert syndrome with ocular defect
    n1=en:Nathalie syndrome | n2=en:joubert syndrome with ocular defect | rel=r_associated | relid=0 | w=21
  583. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:knobloch syndrome
    n1=en:Nathalie syndrome | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=21
  584. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:laurin-sandrow syndrome
    n1=en:Nathalie syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=21
  585. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:lethal congenital contracture syndrome 2
    n1=en:Nathalie syndrome | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=21
  586. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:Nathalie syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=21
  587. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:menkes disease
    n1=en:Nathalie syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=21
  588. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:mesomelic dwarfism reinhardt pfeiffer type
    n1=en:Nathalie syndrome | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=21
  589. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:morm syndrome
    n1=en:Nathalie syndrome | n2=en:morm syndrome | rel=r_associated | relid=0 | w=21
  590. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:norrie syndrome
    n1=en:Nathalie syndrome | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=21
  591. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:pili torti-deafness syndrome
    n1=en:Nathalie syndrome | n2=en:pili torti-deafness syndrome | rel=r_associated | relid=0 | w=21
  592. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:richards-rundle syndrome
    n1=en:Nathalie syndrome | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=21
  593. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:Nathalie syndrome | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=21
  594. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:syndromic orbital border hypoplasia
    n1=en:Nathalie syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=21
  595. en:Nathalie syndrome -- r_associated #0: 21 / 0.618 -> en:verloes bourguignon syndrome
    n1=en:Nathalie syndrome | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=21
≈ 331 relations entrantes

  1. syndrome de Nathalie --- r_associated #0: 30 --> en:Nathalie syndrome
    n1=syndrome de Nathalie | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=30
  2. leucinose --- r_associated #0: 25 --> en:Nathalie syndrome
    n1=leucinose | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=25
  3. Nathalie (syndrome de) --- r_associated #0: 22 --> en:Nathalie syndrome
    n1=Nathalie (syndrome de) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=22
  4. Nathalie --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=Nathalie | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  5. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  6. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  7. en:acid phosphatase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:acid phosphatase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  8. en:acrocallosal syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:acrocallosal syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  9. en:acrodysostosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:acrodysostosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  10. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  11. en:adrenal gland hyperplasia ii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:adrenal gland hyperplasia ii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  12. en:aicardi syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:aicardi syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  13. en:albinism, ocular --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:albinism, ocular | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  14. en:albinotic fundus --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:albinotic fundus | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  15. en:allanson pantzar mcleod syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:allanson pantzar mcleod syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  16. en:allgrove syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:allgrove syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  17. en:alpha-fetoprotein deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:alpha-fetoprotein deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  18. en:aminoacylase 1 deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:aminoacylase 1 deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  19. en:aminomethyltransferase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:aminomethyltransferase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  20. en:andersen syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:andersen syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  21. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  22. en:aplasia of lacrimal and salivary glands --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:aplasia of lacrimal and salivary glands | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  23. en:argininemia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:argininemia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  24. en:arterial tortuosity syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:arterial tortuosity syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  25. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  26. en:atrophoderma vermiculatum --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:atrophoderma vermiculatum | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  27. en:auriculo-condylar syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:auriculo-condylar syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  28. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  29. en:autosomal dominant cystoid macular edema --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal dominant cystoid macular edema | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  30. en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  31. en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal dominant pterygium of conjunctiva | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  32. en:autosomal recessive asexual dwarfism --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal recessive asexual dwarfism | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  33. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  34. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  35. en:autosomal recessive ocular albinism --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal recessive ocular albinism | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  36. en:autosomal recessive primary microcephaly --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:autosomal recessive primary microcephaly | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  37. en:avascular necrosis of femoral head --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:avascular necrosis of femoral head | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  38. en:baller-gerold syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:baller-gerold syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  39. en:bardet-biedl syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:bardet-biedl syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  40. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  41. en:becker generalized myotonia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:becker generalized myotonia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  42. en:behrens baumann dust syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:behrens baumann dust syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  43. en:benign autosomal dominant osteopetrosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:benign autosomal dominant osteopetrosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  44. en:benign congenital myopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:benign congenital myopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  45. en:bifid patella --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:bifid patella | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  46. en:bothnia retinal dystrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:bothnia retinal dystrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  47. en:brachydactyly, type a1 (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:brachydactyly, type a1 (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  48. en:brachymesophalangy 2 and 5 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:brachymesophalangy 2 and 5 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  49. en:brachyphalangia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:brachyphalangia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  50. en:brody myopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:brody myopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  51. en:brown-vialetto-van laere syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:brown-vialetto-van laere syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  52. en:cap myopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cap myopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  53. en:cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  54. en:cataract congenital aggravated --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cataract congenital aggravated | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  55. en:cataract, congenital, cerulean type 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cataract, congenital, cerulean type 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  56. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  57. en:cerebellar ataxia, cayman type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cerebellar ataxia, cayman type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  58. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  59. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  60. en:cerebrotendinous xanthomatosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cerebrotendinous xanthomatosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  61. en:cervical hydromyelocele --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cervical hydromyelocele | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  62. en:charcot-marie-tooth disease type 4 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:charcot-marie-tooth disease type 4 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  63. en:charcot-marie-tooth disease, demyelinating, type 1e --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:charcot-marie-tooth disease, demyelinating, type 1e | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  64. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  65. en:chondrodysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:chondrodysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  66. en:chondrodysplasia punctata syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:chondrodysplasia punctata syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  67. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  68. en:chronic infantile neurological cutaneous and articular syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  69. en:citrin deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:citrin deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  70. en:classical maple syrup urine disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:classical maple syrup urine disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  71. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  72. en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  73. en:cohen syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cohen syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  74. en:col1a1 associated connective tissue disorder --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:col1a1 associated connective tissue disorder | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  75. en:congenital --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  76. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  77. en:congenital ankylosis of elbow --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital ankylosis of elbow | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  78. en:congenital anomaly of carpal bone --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of carpal bone | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  79. en:congenital anomaly of caudal vertebra --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of caudal vertebra | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  80. en:congenital anomaly of humerus --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of humerus | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  81. en:congenital anomaly of lacrimal bone --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of lacrimal bone | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  82. en:congenital anomaly of lumbar vertebra --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of lumbar vertebra | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  83. en:congenital anomaly of metacarpal bone --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of metacarpal bone | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  84. en:congenital anomaly of pelvic bones --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of pelvic bones | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  85. en:congenital anomaly of radius --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of radius | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  86. en:congenital anomaly of rib --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of rib | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  87. en:congenital anomaly of sternebra --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of sternebra | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  88. en:congenital anomaly of tarsal bone --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of tarsal bone | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  89. en:congenital anomaly of thyroid cartilage --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of thyroid cartilage | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  90. en:congenital anomaly of tibia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital anomaly of tibia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  91. en:congenital bowing of long bone --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital bowing of long bone | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  92. en:congenital cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  93. en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  94. en:congenital combined form cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital combined form cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  95. en:congenital disorder of glycosylation type ia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital disorder of glycosylation type ia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  96. en:congenital disorder of glycosylation type ig --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital disorder of glycosylation type ig | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  97. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  98. en:congenital hereditary muscular dystrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital hereditary muscular dystrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  99. en:congenital hypoplasia of clavicle --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital hypoplasia of clavicle | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  100. en:congenital lamellar cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital lamellar cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  101. en:congenital leg bone bowing --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital leg bone bowing | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  102. en:congenital malformation of sternum --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital malformation of sternum | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  103. en:congenital membranous cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital membranous cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  104. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  105. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  106. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  107. en:congenital sutural cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital sutural cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  108. en:congenital transferrin deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital transferrin deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  109. en:congenital valgus ankle --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:congenital valgus ankle | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  110. en:crane-heise syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:crane-heise syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  111. en:craniodiaphyseal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:craniodiaphyseal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  112. en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  113. en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cryptophthalmos syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  114. en:cutis laxa, autosomal dominant --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cutis laxa, autosomal dominant | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  115. en:cutis laxa, autosomal recessive --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cutis laxa, autosomal recessive | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  116. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  117. en:cytochrome-c oxidase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:cytochrome-c oxidase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  118. en:deafness oligodontia syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:deafness oligodontia syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  119. en:deafness-craniofacial syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:deafness-craniofacial syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  120. en:deficiency of fructokinase --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:deficiency of fructokinase | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  121. en:deficiency of glucosyltransferase 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:deficiency of glucosyltransferase 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  122. en:delta phalanx of finger --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:delta phalanx of finger | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  123. en:desmosterolosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:desmosterolosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  124. en:dicarboxylicaminoaciduria --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:dicarboxylicaminoaciduria | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  125. en:dubin-johnson syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:dubin-johnson syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  126. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  127. en:dysostosis multiplex group --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:dysostosis multiplex group | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  128. en:ear, patella, short stature syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:ear, patella, short stature syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  129. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  130. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  131. en:embryonal nuclear cataract (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:embryonal nuclear cataract (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  132. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  133. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  134. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  135. en:factor v and factor viii, combined deficiency of --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:factor v and factor viii, combined deficiency of | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  136. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  137. en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  138. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  139. en:familial interstitial nephritis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial interstitial nephritis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  140. en:familial osteochondritis dissecans --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial osteochondritis dissecans | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  141. en:familial renal iminoglycinuria --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:familial renal iminoglycinuria | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  142. en:farber lipogranulomatosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:farber lipogranulomatosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  143. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  144. en:femur bifid with monodactylous ectrodactyly --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:femur bifid with monodactylous ectrodactyly | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  145. en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:fibrodysplasia ossificans progressiva | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  146. en:freeman-sheldon syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:freeman-sheldon syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  147. en:fronto-facio-nasal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:fronto-facio-nasal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  148. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  149. en:gamma-glutamyltransferase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:gamma-glutamyltransferase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  150. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  151. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  152. en:glutamate formiminotransferase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:glutamate formiminotransferase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  153. en:glycogen storage disease type i --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:glycogen storage disease type i | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  154. en:gracile syndrome (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:gracile syndrome (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  155. en:growth disorders --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:growth disorders | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  156. en:heide syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:heide syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  157. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  158. en:hereditary factor xi deficiency disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary factor xi deficiency disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  159. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  160. en:hereditary multiple exostoses --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary multiple exostoses | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  161. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  162. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  163. en:hereditary vitreoretinopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hereditary vitreoretinopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  164. en:histidinemia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:histidinemia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  165. en:hmg-coa lyase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hmg-coa lyase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  166. en:hnsha due to aldolase a deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hnsha due to aldolase a deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  167. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  168. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  169. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  170. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  171. en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  172. en:hyperimmunoglobulin e syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hyperimmunoglobulin e syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  173. en:hypomagnesemia 1, intestinal --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hypomagnesemia 1, intestinal | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  174. en:hypomyelination and congenital cataract --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hypomyelination and congenital cataract | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  175. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  176. en:inherited arthrogryposis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:inherited arthrogryposis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  177. en:intestinal epithelial dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:intestinal epithelial dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  178. en:isolated congenital alacrima --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:isolated congenital alacrima | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  179. en:isovaleric acidemia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:isovaleric acidemia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  180. en:karandikar maria kamble syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:karandikar maria kamble syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  181. en:klippel-feil syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:klippel-feil syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  182. en:kuskokwim disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:kuskokwim disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  183. en:lactase deficiency, congenital --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:lactase deficiency, congenital | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  184. en:laurence-moon syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:laurence-moon syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  185. en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:lecithin acyltransferase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  186. en:lethal congenital contracture syndrome 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:lethal congenital contracture syndrome 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  187. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  188. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  189. en:leukotriene c4 synthase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:leukotriene c4 synthase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  190. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  191. en:macdermot winter syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:macdermot winter syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  192. en:majeed syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:majeed syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  193. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  194. en:maple syrup urine disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:maple syrup urine disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  195. en:marden-walker syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:marden-walker syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  196. en:marfan syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:marfan syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  197. en:maroteaux-lamy syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:maroteaux-lamy syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  198. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  199. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  200. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  201. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  202. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  203. en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microcephaly deafness syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  204. en:microcephaly, amish type (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microcephaly, amish type (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  205. en:microcephaly-capillary malformation syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  206. en:microphthalmia, syndromic 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microphthalmia, syndromic 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  207. en:microphthalmia, syndromic 3 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microphthalmia, syndromic 3 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  208. en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  209. en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  210. en:mohr-tranebjaerg syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:mohr-tranebjaerg syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  211. en:morquio syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:morquio syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  212. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  213. en:muscle amp deaminase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:muscle amp deaminase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  214. en:muscle atrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:muscle atrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  215. en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  216. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  217. en:myopathy, distal, tateyama type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:myopathy, distal, tateyama type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  218. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  219. en:n-acetylglutamate synthase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:n-acetylglutamate synthase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  220. en:naxos disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:naxos disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  221. en:nemaline myopathy 3 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:nemaline myopathy 3 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  222. en:neonatal progeroid syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:neonatal progeroid syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  223. en:neuroacanthocytosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:neuroacanthocytosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  224. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  225. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  226. en:niemann-pick disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:niemann-pick disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  227. en:noise-induced permanent threshold shift --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:noise-induced permanent threshold shift | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  228. en:non-dystrophic myotonia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:non-dystrophic myotonia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  229. en:nonaka myopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:nonaka myopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  230. en:north american indian childhood cirrhosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:north american indian childhood cirrhosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  231. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  232. en:oculoskeletal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:oculoskeletal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  233. en:orotic aciduria --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:orotic aciduria | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  234. en:osteogenesis imperfecta, levin type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:osteogenesis imperfecta, levin type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  235. en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  236. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  237. en:papillon-lefevre syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:papillon-lefevre syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  238. en:peeling skin syndrome, acral type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:peeling skin syndrome, acral type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  239. en:pelizaeus merzbacher like disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pelizaeus merzbacher like disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  240. en:pentosuria --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pentosuria | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  241. en:peters-plus syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:peters-plus syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  242. en:phenylketonuria ii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:phenylketonuria ii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  243. en:pierre robin syndrome with fetal chondrodysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pierre robin syndrome with fetal chondrodysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  244. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  245. en:polyostotic fibrous dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:polyostotic fibrous dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  246. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  247. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  248. en:prolidase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:prolidase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  249. en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:prolonged electroretinal response suppression | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  250. en:prune belly syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:prune belly syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  251. en:pseudocholinesterase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pseudocholinesterase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  252. en:pseudotrisomy 13 syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  253. en:pulmonary interstitial glycogenosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pulmonary interstitial glycogenosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  254. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  255. en:pyruvate carboxylase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:pyruvate carboxylase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  256. en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  257. en:rapadilino syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:rapadilino syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  258. en:rhizomelic chondrodysplasia punctata --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:rhizomelic chondrodysplasia punctata | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  259. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  260. en:robinow syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:robinow syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  261. en:rubella deafness --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:rubella deafness | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  262. en:sanfilippo syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sanfilippo syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  263. en:sarcosinemia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sarcosinemia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  264. en:schnyder crystalline corneal dystrophy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:schnyder crystalline corneal dystrophy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  265. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  266. en:shwachman-diamond syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:shwachman-diamond syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  267. en:sitosterolemia with xanthomatosis --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sitosterolemia with xanthomatosis | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  268. en:skeletal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:skeletal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  269. en:sly syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sly syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  270. en:smith-mccort dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:smith-mccort dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  271. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  272. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  273. en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  274. en:spondylocamptodactyly --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spondylocamptodactyly | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  275. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  276. en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  277. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  278. en:spondyloepiphyseal dysplasia tarda, x-linked --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  279. en:stickler syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:stickler syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  280. en:stoll levy francfort syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:stoll levy francfort syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  281. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  282. en:sulfite oxidase deficiency --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:sulfite oxidase deficiency | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  283. en:supernumerary vertebra --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:supernumerary vertebra | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  284. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  285. en:tarsal-carpal coalition syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tarsal-carpal coalition syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  286. en:tay-sachs disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tay-sachs disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  287. en:tetra-amelia autosomal recessive --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tetra-amelia autosomal recessive | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  288. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  289. en:thomas syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:thomas syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  290. en:thyroid dyshormonogenesis 4 --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:thyroid dyshormonogenesis 4 | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  291. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  292. en:transitional lumbosacral vertebra --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:transitional lumbosacral vertebra | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  293. en:trichohepatoenteric syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:trichohepatoenteric syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  294. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  295. en:tungland bellman syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tungland bellman syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  296. en:type ii acrocephalopolysyndactyly --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:type ii acrocephalopolysyndactyly | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  297. en:tyrosinemia type ii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tyrosinemia type ii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  298. en:tyrosinemia, type iii --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:tyrosinemia, type iii | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  299. en:uv-sensitive syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:uv-sensitive syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  300. en:valinemia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:valinemia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  301. en:walker-warburg syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:walker-warburg syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  302. en:warsaw breakage syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:warsaw breakage syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  303. en:wellesley carman french syndrome --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:wellesley carman french syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  304. en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  305. en:wolman disease --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:wolman disease | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  306. en:x-linked retinal dysplasia --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:x-linked retinal dysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  307. en:xanthinuria, type i --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=en:xanthinuria, type i | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  308. syndrome de surdité neurosensorielle-paralysie ponto-bulbaire --- r_associated #0: 20 --> en:Nathalie syndrome
    n1=syndrome de surdité neurosensorielle-paralysie ponto-bulbaire | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  309. aclasie diaphysaire --- r_associated #0: 15 --> en:Nathalie syndrome
    n1=aclasie diaphysaire | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=15
  310. déficit en céto-acide décarboxylase --- r_associated #0: 15 --> en:Nathalie syndrome
    n1=déficit en céto-acide décarboxylase | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=15
  311. exostose héréditaire multiple --- r_associated #0: 15 --> en:Nathalie syndrome
    n1=exostose héréditaire multiple | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=15
  312. amyotrophie --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=amyotrophie | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  313. atrophie des muscles --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=atrophie des muscles | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  314. atrophie musculaire --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=atrophie musculaire | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  315. chondrodysplasia --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=chondrodysplasia | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  316. chondrodysplasie déformante héréditaire --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=chondrodysplasie déformante héréditaire | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  317. dysplasie enchondrale --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=dysplasie enchondrale | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  318. déficit en cytochrome oxydase --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=déficit en cytochrome oxydase | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  319. fonte musculaire --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=fonte musculaire | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  320. maladie de Bessel-Hagen --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=maladie de Bessel-Hagen | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  321. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  322. maladie du sirop d'érable --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=maladie du sirop d'érable | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  323. maladie exostosante multiple --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=maladie exostosante multiple | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  324. maladie ostéogénique --- r_associated #0: 10 --> en:Nathalie syndrome
    n1=maladie ostéogénique | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=10
  325. chondrodysplasie héréditaire déformante --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=chondrodysplasie héréditaire déformante | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  326. maladie de Wolman --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=maladie de Wolman | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  327. maladie des exostoses multiples --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=maladie des exostoses multiples | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  328. maladie des urines avec odeur de sirop erable --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=maladie des urines avec odeur de sirop erable | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  329. myatrophie --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=myatrophie | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  330. natrémie --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=natrémie | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=5
  331. syndrome de Stickler --- r_associated #0: 5 --> en:Nathalie syndrome
    n1=syndrome de Stickler | n2=en:Nathalie syndrome | 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