Javascript doit fonctionner ! Activez-le et rechargez cette page.
Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
• Consolider
le terme
  Options  
             

  Filtrage type relations : +   - (ex: 4, 12, 18, 36, 444, 555, 777)
  Filtrage valeur :          min   max
  Filtrage type noeuds :   +   - (ex: 4, 6, 8, 9, 10, 12, 18, 36, 444, 555, 777)

  Présentation de sortie :   (ex: -rien-, cloud, nicecloud)
 

'Goltz (syndrome de)'
(id=16867217 ; fe=Goltz (syndrome de) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=11400 creation date=2021-07-25 touchdate=2025-08-27 17:19:37.000)
≈ 872 relations sortantes

  1. Goltz (syndrome de) -- r_associated #0: 71 / 1 -> Goltz
    n1=Goltz (syndrome de) | n2=Goltz | rel=r_associated | relid=0 | w=71
  2. Goltz (syndrome de) -- r_associated #0: 64 / 0.901 -> syndrome
    n1=Goltz (syndrome de) | n2=syndrome | rel=r_associated | relid=0 | w=64
  3. Goltz (syndrome de) -- r_associated #0: 45 / 0.634 -> ostéopathie striée
    n1=Goltz (syndrome de) | n2=ostéopathie striée | rel=r_associated | relid=0 | w=45
  4. Goltz (syndrome de) -- r_associated #0: 40 / 0.563 -> hamartome angiolipomateux de Howell
    n1=Goltz (syndrome de) | n2=hamartome angiolipomateux de Howell | rel=r_associated | relid=0 | w=40
  5. Goltz (syndrome de) -- r_associated #0: 35 / 0.493 -> hypoplasie dermique focale
    n1=Goltz (syndrome de) | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=35
  6. Goltz (syndrome de) -- r_associated #0: 32 / 0.451 -> en:focal dermal hypoplasia
    n1=Goltz (syndrome de) | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=32
  7. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=Goltz (syndrome de) | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=30
  8. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:abetalipoproteinemia
    n1=Goltz (syndrome de) | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=30
  9. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:absent toenails
    n1=Goltz (syndrome de) | n2=en:absent toenails | rel=r_associated | relid=0 | w=30
  10. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:acrodermatitis enteropathica
    n1=Goltz (syndrome de) | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=30
  11. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:adolescent x-linked adrenoleukodystrophy
    n1=Goltz (syndrome de) | n2=en:adolescent x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=30
  12. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:allgrove syndrome
    n1=Goltz (syndrome de) | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=30
  13. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:analbuminemia
    n1=Goltz (syndrome de) | n2=en:analbuminemia | rel=r_associated | relid=0 | w=30
  14. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:andersen syndrome
    n1=Goltz (syndrome de) | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=30
  15. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:anhydrotic ectodermal dysplasias
    n1=Goltz (syndrome de) | n2=en:anhydrotic ectodermal dysplasias | rel=r_associated | relid=0 | w=30
  16. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:anophthalmos
    n1=Goltz (syndrome de) | n2=en:anophthalmos | rel=r_associated | relid=0 | w=30
  17. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:arakawa syndrome ii
    n1=Goltz (syndrome de) | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=30
  18. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:bernard-soulier syndrome
    n1=Goltz (syndrome de) | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=30
  19. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:brugsch's syndrome
    n1=Goltz (syndrome de) | n2=en:brugsch's syndrome | rel=r_associated | relid=0 | w=30
  20. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:carnitine palmitoyltransferase ii deficiency
    n1=Goltz (syndrome de) | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=30
  21. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:cleft ala nasi
    n1=Goltz (syndrome de) | n2=en:cleft ala nasi | rel=r_associated | relid=0 | w=30
  22. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:codas syndrome
    n1=Goltz (syndrome de) | n2=en:codas syndrome | rel=r_associated | relid=0 | w=30
  23. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:congenital amegakaryocytic thrombocytopenia
    n1=Goltz (syndrome de) | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=30
  24. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:congenital anomaly of hair
    n1=Goltz (syndrome de) | n2=en:congenital anomaly of hair | rel=r_associated | relid=0 | w=30
  25. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:congenital ichthyosis
    n1=Goltz (syndrome de) | n2=en:congenital ichthyosis | rel=r_associated | relid=0 | w=30
  26. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:cowden syndrome
    n1=Goltz (syndrome de) | n2=en:cowden syndrome | rel=r_associated | relid=0 | w=30
  27. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:cranioectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=30
  28. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:d-bifunctional protein deficiency
    n1=Goltz (syndrome de) | n2=en:d-bifunctional protein deficiency | rel=r_associated | relid=0 | w=30
  29. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:deafness, autosomal recessive 1a
    n1=Goltz (syndrome de) | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=30
  30. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:dent's disease
    n1=Goltz (syndrome de) | n2=en:dent's disease | rel=r_associated | relid=0 | w=30
  31. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:drug- and toxin-induced pulmonary arterial hypertension
    n1=Goltz (syndrome de) | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=30
  32. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:dyschromatosis symmetrica hereditaria
    n1=Goltz (syndrome de) | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=30
  33. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:ectodermal dysplasia with tooth-sweating defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with tooth-sweating defect | rel=r_associated | relid=0 | w=30
  34. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:ectrodactyly
    n1=Goltz (syndrome de) | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=30
  35. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:epidemiologic
    n1=Goltz (syndrome de) | n2=en:epidemiologic | rel=r_associated | relid=0 | w=30
  36. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:epidermodysplasia verruciformis
    n1=Goltz (syndrome de) | n2=en:epidermodysplasia verruciformis | rel=r_associated | relid=0 | w=30
  37. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:erythromelalgia
    n1=Goltz (syndrome de) | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=30
  38. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:ethnologic
    n1=Goltz (syndrome de) | n2=en:ethnologic | rel=r_associated | relid=0 | w=30
  39. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:fatal familial insomnia
    n1=Goltz (syndrome de) | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=30
  40. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:focal facial dermal dysplasia
    n1=Goltz (syndrome de) | n2=en:focal facial dermal dysplasia | rel=r_associated | relid=0 | w=30
  41. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:frontotemporal dementia
    n1=Goltz (syndrome de) | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
  42. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:glanzmann thrombasthenia
    n1=Goltz (syndrome de) | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=30
  43. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:glutaric acidemia type 1
    n1=Goltz (syndrome de) | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=30
  44. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:goldenhar syndrome
    n1=Goltz (syndrome de) | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=30
  45. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:hereditary coproporphyria
    n1=Goltz (syndrome de) | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=30
  46. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:hereditary hemorrhagic telangiectasia
    n1=Goltz (syndrome de) | n2=en:hereditary hemorrhagic telangiectasia | rel=r_associated | relid=0 | w=30
  47. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:hypokalemic periodic paralysis
    n1=Goltz (syndrome de) | n2=en:hypokalemic periodic paralysis | rel=r_associated | relid=0 | w=30
  48. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:leptospirosis
    n1=Goltz (syndrome de) | n2=en:leptospirosis | rel=r_associated | relid=0 | w=30
  49. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:lesch-nyhan syndrome
    n1=Goltz (syndrome de) | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=30
  50. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:leukodystrophy
    n1=Goltz (syndrome de) | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=30
  51. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:levocardia
    n1=Goltz (syndrome de) | n2=en:levocardia | rel=r_associated | relid=0 | w=30
  52. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:low set ears
    n1=Goltz (syndrome de) | n2=en:low set ears | rel=r_associated | relid=0 | w=30
  53. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:lysosomal storage disease
    n1=Goltz (syndrome de) | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=30
  54. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:masa syndrome (disorder)
    n1=Goltz (syndrome de) | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=30
  55. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:meesmann corneal dystrophy
    n1=Goltz (syndrome de) | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=30
  56. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:mixed connective tissue disease
    n1=Goltz (syndrome de) | n2=en:mixed connective tissue disease | rel=r_associated | relid=0 | w=30
  57. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:myelomeningocele
    n1=Goltz (syndrome de) | n2=en:myelomeningocele | rel=r_associated | relid=0 | w=30
  58. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:myokymia
    n1=Goltz (syndrome de) | n2=en:myokymia | rel=r_associated | relid=0 | w=30
  59. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:neuromyelitis optica
    n1=Goltz (syndrome de) | n2=en:neuromyelitis optica | rel=r_associated | relid=0 | w=30
  60. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:pancreatic lipase deficiency
    n1=Goltz (syndrome de) | n2=en:pancreatic lipase deficiency | rel=r_associated | relid=0 | w=30
  61. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:partington x-linked mental retardation syndrome
    n1=Goltz (syndrome de) | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30
  62. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:pearson marrow-pancreas syndrome
    n1=Goltz (syndrome de) | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=30
  63. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:porphyria cutanea tarda
    n1=Goltz (syndrome de) | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=30
  64. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:primary carnitine deficiency
    n1=Goltz (syndrome de) | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=30
  65. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:progressive muscular atrophy
    n1=Goltz (syndrome de) | n2=en:progressive muscular atrophy | rel=r_associated | relid=0 | w=30
  66. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:pseudoxanthoma elasticum
    n1=Goltz (syndrome de) | n2=en:pseudoxanthoma elasticum | rel=r_associated | relid=0 | w=30
  67. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:radiotherapeutic
    n1=Goltz (syndrome de) | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=30
  68. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:septo-optic dysplasia
    n1=Goltz (syndrome de) | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=30
  69. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:simple syndactyly of fingers - second to fourth web
    n1=Goltz (syndrome de) | n2=en:simple syndactyly of fingers - second to fourth web | rel=r_associated | relid=0 | w=30
  70. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:smith-lemli-opitz syndrome
    n1=Goltz (syndrome de) | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=30
  71. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:stiff skin syndrome
    n1=Goltz (syndrome de) | n2=en:stiff skin syndrome | rel=r_associated | relid=0 | w=30
  72. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:subacute sclerosing panencephalitis
    n1=Goltz (syndrome de) | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=30
  73. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:sudden unexplained death in childhood
    n1=Goltz (syndrome de) | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=30
  74. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:syndactyly (75%)
    n1=Goltz (syndrome de) | n2=en:syndactyly (75%) | rel=r_associated | relid=0 | w=30
  75. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:syndactyly of toes without bone fusion
    n1=Goltz (syndrome de) | n2=en:syndactyly of toes without bone fusion | rel=r_associated | relid=0 | w=30
  76. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:takotsubo cardiomyopathy
    n1=Goltz (syndrome de) | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=30
  77. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:therapeutic aspects
    n1=Goltz (syndrome de) | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=30
  78. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:triploidy syndrome
    n1=Goltz (syndrome de) | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=30
  79. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:true hermaphroditism
    n1=Goltz (syndrome de) | n2=en:true hermaphroditism | rel=r_associated | relid=0 | w=30
  80. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:viruses
    n1=Goltz (syndrome de) | n2=en:viruses | rel=r_associated | relid=0 | w=30
  81. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:wallerian degeneration
    n1=Goltz (syndrome de) | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=30
  82. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:wandering spleen
    n1=Goltz (syndrome de) | n2=en:wandering spleen | rel=r_associated | relid=0 | w=30
  83. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:x-linked retinal dysplasia
    n1=Goltz (syndrome de) | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=30
  84. Goltz (syndrome de) -- r_associated #0: 30 / 0.423 -> en:x-linked severe combined immunodeficiency
    n1=Goltz (syndrome de) | n2=en:x-linked severe combined immunodeficiency | rel=r_associated | relid=0 | w=30
  85. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:1p36 deletion syndrome
    n1=Goltz (syndrome de) | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=29
  86. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:acrocephalosyndactyly
    n1=Goltz (syndrome de) | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=29
  87. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:affected males are all result of new mutation
    n1=Goltz (syndrome de) | n2=en:affected males are all result of new mutation | rel=r_associated | relid=0 | w=29
  88. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:aicardi syndrome
    n1=Goltz (syndrome de) | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=29
  89. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:allan-herndon-dudley syndrome
    n1=Goltz (syndrome de) | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=29
  90. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:aniridia
    n1=Goltz (syndrome de) | n2=en:aniridia | rel=r_associated | relid=0 | w=29
  91. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:arnold-chiari malformation
    n1=Goltz (syndrome de) | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=29
  92. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:aspects of mortality statistics
    n1=Goltz (syndrome de) | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=29
  93. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:biotinidase deficiency
    n1=Goltz (syndrome de) | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=29
  94. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:birthmark
    n1=Goltz (syndrome de) | n2=en:birthmark | rel=r_associated | relid=0 | w=29
  95. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:brachydactyly (60%)
    n1=Goltz (syndrome de) | n2=en:brachydactyly (60%) | rel=r_associated | relid=0 | w=29
  96. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:charge syndrome
    n1=Goltz (syndrome de) | n2=en:charge syndrome | rel=r_associated | relid=0 | w=29
  97. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:congenital cortical hyperostosis
    n1=Goltz (syndrome de) | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=29
  98. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:congenital insensitivity to pain with anhidrosis
    n1=Goltz (syndrome de) | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=29
  99. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:congenital phimosis
    n1=Goltz (syndrome de) | n2=en:congenital phimosis | rel=r_associated | relid=0 | w=29
  100. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:craniofacial dysostosis
    n1=Goltz (syndrome de) | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=29
  101. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:cystathioninuria
    n1=Goltz (syndrome de) | n2=en:cystathioninuria | rel=r_associated | relid=0 | w=29
  102. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:deletion 18p syndrome
    n1=Goltz (syndrome de) | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=29
  103. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:dentinogenesis imperfecta
    n1=Goltz (syndrome de) | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=29
  104. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:diastasis recti
    n1=Goltz (syndrome de) | n2=en:diastasis recti | rel=r_associated | relid=0 | w=29
  105. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=29
  106. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:dmd-associated dilated cardiomyopathy
    n1=Goltz (syndrome de) | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=29
  107. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:ectodermal dysplasia with hair-tooth-nail-sweating defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with hair-tooth-nail-sweating defect | rel=r_associated | relid=0 | w=29
  108. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:ellis-van creveld syndrome
    n1=Goltz (syndrome de) | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=29
  109. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:embryologic
    n1=Goltz (syndrome de) | n2=en:embryologic | rel=r_associated | relid=0 | w=29
  110. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:etiology aspects
    n1=Goltz (syndrome de) | n2=en:etiology aspects | rel=r_associated | relid=0 | w=29
  111. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:familial hypertrophic cardiomyopathy
    n1=Goltz (syndrome de) | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=29
  112. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:gastric antral vascular ectasia
    n1=Goltz (syndrome de) | n2=en:gastric antral vascular ectasia | rel=r_associated | relid=0 | w=29
  113. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:genetic aspects
    n1=Goltz (syndrome de) | n2=en:genetic aspects | rel=r_associated | relid=0 | w=29
  114. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:gray platelet syndrome
    n1=Goltz (syndrome de) | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=29
  115. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hellp syndrome
    n1=Goltz (syndrome de) | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=29
  116. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hemophilia b
    n1=Goltz (syndrome de) | n2=en:hemophilia b | rel=r_associated | relid=0 | w=29
  117. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:heterotaxy syndrome
    n1=Goltz (syndrome de) | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=29
  118. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hidrotic ectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:hidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=29
  119. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hooded penis
    n1=Goltz (syndrome de) | n2=en:hooded penis | rel=r_associated | relid=0 | w=29
  120. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hydrocephalus
    n1=Goltz (syndrome de) | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=29
  121. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:hyper-igm immunodeficiency syndrome, type 1
    n1=Goltz (syndrome de) | n2=en:hyper-igm immunodeficiency syndrome, type 1 | rel=r_associated | relid=0 | w=29
  122. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:jacobsen syndrome
    n1=Goltz (syndrome de) | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=29
  123. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:leopard syndrome
    n1=Goltz (syndrome de) | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=29
  124. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:leri-weill dyschondrosteosis
    n1=Goltz (syndrome de) | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=29
  125. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:loeys-dietz syndrome
    n1=Goltz (syndrome de) | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=29
  126. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=29
  127. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:maffucci syndrome
    n1=Goltz (syndrome de) | n2=en:maffucci syndrome | rel=r_associated | relid=0 | w=29
  128. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:malformations of cortical development
    n1=Goltz (syndrome de) | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=29
  129. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:mansonelliasis
    n1=Goltz (syndrome de) | n2=en:mansonelliasis | rel=r_associated | relid=0 | w=29
  130. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:marburg virus disease
    n1=Goltz (syndrome de) | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=29
  131. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=29
  132. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:meningeal tuberculosis
    n1=Goltz (syndrome de) | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=29
  133. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:methionine adenosyltransferase deficiency
    n1=Goltz (syndrome de) | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=29
  134. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:microphthalmia, syndromic 2
    n1=Goltz (syndrome de) | n2=en:microphthalmia, syndromic 2 | rel=r_associated | relid=0 | w=29
  135. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:mohr-tranebjaerg syndrome
    n1=Goltz (syndrome de) | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=29
  136. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:n-acetylglutamate synthase deficiency
    n1=Goltz (syndrome de) | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=29
  137. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:nail-patella syndrome
    n1=Goltz (syndrome de) | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=29
  138. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:norrie syndrome
    n1=Goltz (syndrome de) | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=29
  139. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:oculo-dento-digital syndrome
    n1=Goltz (syndrome de) | n2=en:oculo-dento-digital syndrome | rel=r_associated | relid=0 | w=29
  140. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:optic neuritis
    n1=Goltz (syndrome de) | n2=en:optic neuritis | rel=r_associated | relid=0 | w=29
  141. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:osteochondrodysplasia
    n1=Goltz (syndrome de) | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=29
  142. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:otopalatodigital syndrome type 1
    n1=Goltz (syndrome de) | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=29
  143. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:peritoneal panniculitis
    n1=Goltz (syndrome de) | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=29
  144. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:phosphoenolpyruvate carboxykinase deficiency
    n1=Goltz (syndrome de) | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=29
  145. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:poland syndrome
    n1=Goltz (syndrome de) | n2=en:poland syndrome | rel=r_associated | relid=0 | w=29
  146. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:porcn, 13-bp dup, nt1059
    n1=Goltz (syndrome de) | n2=en:porcn, 13-bp dup, nt1059 | rel=r_associated | relid=0 | w=29
  147. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:porcn, 178g-a, gly60arg
    n1=Goltz (syndrome de) | n2=en:porcn, 178g-a, gly60arg | rel=r_associated | relid=0 | w=29
  148. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:proteus-like syndrome (disorder)
    n1=Goltz (syndrome de) | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=29
  149. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:rett syndrome
    n1=Goltz (syndrome de) | n2=en:rett syndrome | rel=r_associated | relid=0 | w=29
  150. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:seckel syndrome
    n1=Goltz (syndrome de) | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=29
  151. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:selective antibody deficiency with normal immunoglobulins
    n1=Goltz (syndrome de) | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=29
  152. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:simple syndactyly of fingers - first web
    n1=Goltz (syndrome de) | n2=en:simple syndactyly of fingers - first web | rel=r_associated | relid=0 | w=29
  153. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:sitosterolemia
    n1=Goltz (syndrome de) | n2=en:sitosterolemia | rel=r_associated | relid=0 | w=29
  154. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:syndactyly of fingers
    n1=Goltz (syndrome de) | n2=en:syndactyly of fingers | rel=r_associated | relid=0 | w=29
  155. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:taxonomic
    n1=Goltz (syndrome de) | n2=en:taxonomic | rel=r_associated | relid=0 | w=29
  156. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:thyroid dysgenesis
    n1=Goltz (syndrome de) | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=29
  157. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:treacher collins syndrome
    n1=Goltz (syndrome de) | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=29
  158. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:uveomeningoencephalitic syndrome
    n1=Goltz (syndrome de) | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=29
  159. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:x-linked creatine transporter deficiency
    n1=Goltz (syndrome de) | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=29
  160. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:xeroderma pigmentosum
    n1=Goltz (syndrome de) | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=29
  161. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> en:yellow nail syndrome
    n1=Goltz (syndrome de) | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=29
  162. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> hypoplasie dermique en aires
    n1=Goltz (syndrome de) | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=29
  163. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> médecine
    n1=Goltz (syndrome de) | n2=médecine | rel=r_associated | relid=0 | w=29
  164. Goltz (syndrome de) -- r_associated #0: 29 / 0.408 -> syndrome d'hypoplasie dermique en aires
    n1=Goltz (syndrome de) | n2=syndrome d'hypoplasie dermique en aires | rel=r_associated | relid=0 | w=29
  165. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:absence of toe
    n1=Goltz (syndrome de) | n2=en:absence of toe | rel=r_associated | relid=0 | w=28
  166. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:achromatopsia
    n1=Goltz (syndrome de) | n2=en:achromatopsia | rel=r_associated | relid=0 | w=28
  167. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:agnosia
    n1=Goltz (syndrome de) | n2=en:agnosia | rel=r_associated | relid=0 | w=28
  168. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:ainhum
    n1=Goltz (syndrome de) | n2=en:ainhum | rel=r_associated | relid=0 | w=28
  169. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:alkaptonuria
    n1=Goltz (syndrome de) | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=28
  170. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:amaurosis fugax
    n1=Goltz (syndrome de) | n2=en:amaurosis fugax | rel=r_associated | relid=0 | w=28
  171. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:androgen insensitivity syndrome
    n1=Goltz (syndrome de) | n2=en:androgen insensitivity syndrome | rel=r_associated | relid=0 | w=28
  172. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:autoimmune polyendocrinopathy syndrome
    n1=Goltz (syndrome de) | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=28
  173. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:bartter syndrome
    n1=Goltz (syndrome de) | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=28
  174. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:beta-methylcrotonylglycinuria
    n1=Goltz (syndrome de) | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=28
  175. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:caroli disease
    n1=Goltz (syndrome de) | n2=en:caroli disease | rel=r_associated | relid=0 | w=28
  176. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:cartilage hair hypoplasia
    n1=Goltz (syndrome de) | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=28
  177. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:chilblains
    n1=Goltz (syndrome de) | n2=en:chilblains | rel=r_associated | relid=0 | w=28
  178. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:complication aspects
    n1=Goltz (syndrome de) | n2=en:complication aspects | rel=r_associated | relid=0 | w=28
  179. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:congenital parameatal cyst
    n1=Goltz (syndrome de) | n2=en:congenital parameatal cyst | rel=r_associated | relid=0 | w=28
  180. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:congenital scar
    n1=Goltz (syndrome de) | n2=en:congenital scar | rel=r_associated | relid=0 | w=28
  181. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:cor triatriatum
    n1=Goltz (syndrome de) | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=28
  182. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:cutaneous lesion resulting from spinal dysraphism
    n1=Goltz (syndrome de) | n2=en:cutaneous lesion resulting from spinal dysraphism | rel=r_associated | relid=0 | w=28
  183. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:d-glyceric aciduria
    n1=Goltz (syndrome de) | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=28
  184. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:darier disease
    n1=Goltz (syndrome de) | n2=en:darier disease | rel=r_associated | relid=0 | w=28
  185. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:double eyebrow
    n1=Goltz (syndrome de) | n2=en:double eyebrow | rel=r_associated | relid=0 | w=28
  186. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:dysplastic cerebellar gangliocytoma
    n1=Goltz (syndrome de) | n2=en:dysplastic cerebellar gangliocytoma | rel=r_associated | relid=0 | w=28
  187. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:ectodermal dysplasia with tooth-nail defects
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with tooth-nail defects | rel=r_associated | relid=0 | w=28
  188. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:ectopia lentis (6%)
    n1=Goltz (syndrome de) | n2=en:ectopia lentis (6%) | rel=r_associated | relid=0 | w=28
  189. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:felty syndrome
    n1=Goltz (syndrome de) | n2=en:felty syndrome | rel=r_associated | relid=0 | w=28
  190. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:fibrodysplasia ossificans progressiva
    n1=Goltz (syndrome de) | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=28
  191. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:frontonasal dysplasia
    n1=Goltz (syndrome de) | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=28
  192. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:gerstmann-straussler-scheinker disease
    n1=Goltz (syndrome de) | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=28
  193. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:hamartoma
    n1=Goltz (syndrome de) | n2=en:hamartoma | rel=r_associated | relid=0 | w=28
  194. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:hard skin syndrome parana type
    n1=Goltz (syndrome de) | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=28
  195. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:hereditary mucosal leukokeratosis
    n1=Goltz (syndrome de) | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=28
  196. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:holt-oram syndrome
    n1=Goltz (syndrome de) | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=28
  197. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=Goltz (syndrome de) | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=28
  198. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:infantile neuroaxonal dystrophy
    n1=Goltz (syndrome de) | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=28
  199. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:kirman syndrome
    n1=Goltz (syndrome de) | n2=en:kirman syndrome | rel=r_associated | relid=0 | w=28
  200. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:landau-kleffner syndrome
    n1=Goltz (syndrome de) | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=28
  201. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:leprosy
    n1=Goltz (syndrome de) | n2=en:leprosy | rel=r_associated | relid=0 | w=28
  202. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:liddle syndrome
    n1=Goltz (syndrome de) | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=28
  203. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:lubs x-linked mental retardation syndrome
    n1=Goltz (syndrome de) | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
  204. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:lumpy scalp syndrome
    n1=Goltz (syndrome de) | n2=en:lumpy scalp syndrome | rel=r_associated | relid=0 | w=28
  205. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:maple syrup urine disease
    n1=Goltz (syndrome de) | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=28
  206. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:meckel-gruber syndrome
    n1=Goltz (syndrome de) | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=28
  207. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:melkersson-rosenthal syndrome
    n1=Goltz (syndrome de) | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=28
  208. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:menkes disease
    n1=Goltz (syndrome de) | n2=en:menkes disease | rel=r_associated | relid=0 | w=28
  209. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:molybdenum cofactor deficiency
    n1=Goltz (syndrome de) | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=28
  210. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:neonatal progeroid syndrome
    n1=Goltz (syndrome de) | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=28
  211. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:neuronal intranuclear inclusion disease
    n1=Goltz (syndrome de) | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=28
  212. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:nystagmus
    n1=Goltz (syndrome de) | n2=en:nystagmus | rel=r_associated | relid=0 | w=28
  213. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:ocular albinism, type ii
    n1=Goltz (syndrome de) | n2=en:ocular albinism, type ii | rel=r_associated | relid=0 | w=28
  214. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:oligodactyly (45%)
    n1=Goltz (syndrome de) | n2=en:oligodactyly (45%) | rel=r_associated | relid=0 | w=28
  215. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:papillomatosis
    n1=Goltz (syndrome de) | n2=en:papillomatosis | rel=r_associated | relid=0 | w=28
  216. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:pemphigoid gestationis
    n1=Goltz (syndrome de) | n2=en:pemphigoid gestationis | rel=r_associated | relid=0 | w=28
  217. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:pityriasis lichenoides
    n1=Goltz (syndrome de) | n2=en:pityriasis lichenoides | rel=r_associated | relid=0 | w=28
  218. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:pityriasis rubra pilaris
    n1=Goltz (syndrome de) | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=28
  219. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:polydactyly, postaxial
    n1=Goltz (syndrome de) | n2=en:polydactyly, postaxial | rel=r_associated | relid=0 | w=28
  220. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:porokeratosis, disseminated superficial actinic
    n1=Goltz (syndrome de) | n2=en:porokeratosis, disseminated superficial actinic | rel=r_associated | relid=0 | w=28
  221. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:prekallikrein deficiency
    n1=Goltz (syndrome de) | n2=en:prekallikrein deficiency | rel=r_associated | relid=0 | w=28
  222. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:prosopagnosia
    n1=Goltz (syndrome de) | n2=en:prosopagnosia | rel=r_associated | relid=0 | w=28
  223. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:pseudotumor cerebri
    n1=Goltz (syndrome de) | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=28
  224. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:pterygium colli
    n1=Goltz (syndrome de) | n2=en:pterygium colli | rel=r_associated | relid=0 | w=28
  225. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:scoliosis
    n1=Goltz (syndrome de) | n2=en:scoliosis | rel=r_associated | relid=0 | w=28
  226. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:sea-blue histiocyte syndrome
    n1=Goltz (syndrome de) | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=28
  227. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:short ribs
    n1=Goltz (syndrome de) | n2=en:short ribs | rel=r_associated | relid=0 | w=28
  228. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:short stature
    n1=Goltz (syndrome de) | n2=en:short stature | rel=r_associated | relid=0 | w=28
  229. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:shy-drager syndrome
    n1=Goltz (syndrome de) | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=28
  230. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:skin atrophy
    n1=Goltz (syndrome de) | n2=en:skin atrophy | rel=r_associated | relid=0 | w=28
  231. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:spondyloepiphyseal dysplasia tarda, x-linked
    n1=Goltz (syndrome de) | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=28
  232. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:sweet syndrome
    n1=Goltz (syndrome de) | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=28
  233. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:undescended testes
    n1=Goltz (syndrome de) | n2=en:undescended testes | rel=r_associated | relid=0 | w=28
  234. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:uniparental disomy
    n1=Goltz (syndrome de) | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=28
  235. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:urticaria pigmentosa/maculopapular cutaneous mastocytosis
    n1=Goltz (syndrome de) | n2=en:urticaria pigmentosa/maculopapular cutaneous mastocytosis | rel=r_associated | relid=0 | w=28
  236. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:waisman syndrome
    n1=Goltz (syndrome de) | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=28
  237. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:whipple disease
    n1=Goltz (syndrome de) | n2=en:whipple disease | rel=r_associated | relid=0 | w=28
  238. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:x-linked adrenal hypoplasia congenita
    n1=Goltz (syndrome de) | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=28
  239. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:x-linked hydrocephalus syndrome
    n1=Goltz (syndrome de) | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=28
  240. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia
    n1=Goltz (syndrome de) | n2=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | rel=r_associated | relid=0 | w=28
  241. Goltz (syndrome de) -- r_associated #0: 28 / 0.394 -> syndrome de
    n1=Goltz (syndrome de) | n2=syndrome de | rel=r_associated | relid=0 | w=28
  242. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> dermique
    n1=Goltz (syndrome de) | n2=dermique | rel=r_associated | relid=0 | w=27
  243. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:aniridia (3%)
    n1=Goltz (syndrome de) | n2=en:aniridia (3%) | rel=r_associated | relid=0 | w=27
  244. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:aprosencephaly
    n1=Goltz (syndrome de) | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=27
  245. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:argininemia
    n1=Goltz (syndrome de) | n2=en:argininemia | rel=r_associated | relid=0 | w=27
  246. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:argininosuccinic aciduria
    n1=Goltz (syndrome de) | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=27
  247. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:arrhythmogenic right ventricular dysplasia
    n1=Goltz (syndrome de) | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=27
  248. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:broad nasal tip
    n1=Goltz (syndrome de) | n2=en:broad nasal tip | rel=r_associated | relid=0 | w=27
  249. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:centrofacial lentiginosis syndrome
    n1=Goltz (syndrome de) | n2=en:centrofacial lentiginosis syndrome | rel=r_associated | relid=0 | w=27
  250. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:childhood cerebral x-linked adrenoleukodystrophy
    n1=Goltz (syndrome de) | n2=en:childhood cerebral x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=27
  251. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:chondrodysplasia punctata
    n1=Goltz (syndrome de) | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=27
  252. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:coffin-lowry syndrome
    n1=Goltz (syndrome de) | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=27
  253. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:combined lipase deficiency
    n1=Goltz (syndrome de) | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=27
  254. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:congenital abnormality
    n1=Goltz (syndrome de) | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=27
  255. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:congenital fecal fistula
    n1=Goltz (syndrome de) | n2=en:congenital fecal fistula | rel=r_associated | relid=0 | w=27
  256. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:congenital hyperplasia of sebaceous glands of lip
    n1=Goltz (syndrome de) | n2=en:congenital hyperplasia of sebaceous glands of lip | rel=r_associated | relid=0 | w=27
  257. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:congenital myasthenic syndrome
    n1=Goltz (syndrome de) | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=27
  258. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:congenital pigmentary skin anomalies
    n1=Goltz (syndrome de) | n2=en:congenital pigmentary skin anomalies | rel=r_associated | relid=0 | w=27
  259. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:dermal sinus
    n1=Goltz (syndrome de) | n2=en:dermal sinus | rel=r_associated | relid=0 | w=27
  260. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:diagnosis aspect
    n1=Goltz (syndrome de) | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=27
  261. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:distichiasis
    n1=Goltz (syndrome de) | n2=en:distichiasis | rel=r_associated | relid=0 | w=27
  262. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:dyskeratosis congenita
    n1=Goltz (syndrome de) | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=27
  263. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:dysostosis
    n1=Goltz (syndrome de) | n2=en:dysostosis | rel=r_associated | relid=0 | w=27
  264. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ectodermal dysplasia with hair-nail defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with hair-nail defect | rel=r_associated | relid=0 | w=27
  265. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ectodermal dysplasia with hair-tooth defects
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with hair-tooth defects | rel=r_associated | relid=0 | w=27
  266. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ectodermal dysplasia with hair-tooth-nail defects
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with hair-tooth-nail defects | rel=r_associated | relid=0 | w=27
  267. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:erythrokeratodermia variabilis
    n1=Goltz (syndrome de) | n2=en:erythrokeratodermia variabilis | rel=r_associated | relid=0 | w=27
  268. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:erythropoietic porphyria
    n1=Goltz (syndrome de) | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=27
  269. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:gangrenous stomatitis
    n1=Goltz (syndrome de) | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=27
  270. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:generalized abnormality of skin
    n1=Goltz (syndrome de) | n2=en:generalized abnormality of skin | rel=r_associated | relid=0 | w=27
  271. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:genitoperineal raphe cyst
    n1=Goltz (syndrome de) | n2=en:genitoperineal raphe cyst | rel=r_associated | relid=0 | w=27
  272. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:genu varum
    n1=Goltz (syndrome de) | n2=en:genu varum | rel=r_associated | relid=0 | w=27
  273. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:glycogen storage disease type iib
    n1=Goltz (syndrome de) | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=27
  274. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:glycogen storage disease type viii
    n1=Goltz (syndrome de) | n2=en:glycogen storage disease type viii | rel=r_associated | relid=0 | w=27
  275. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hallermann syndrome
    n1=Goltz (syndrome de) | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=27
  276. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hemangiomatosis with thrombocytopenia
    n1=Goltz (syndrome de) | n2=en:hemangiomatosis with thrombocytopenia | rel=r_associated | relid=0 | w=27
  277. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hemochromatosis
    n1=Goltz (syndrome de) | n2=en:hemochromatosis | rel=r_associated | relid=0 | w=27
  278. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hyperpipecolatemia
    n1=Goltz (syndrome de) | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=27
  279. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hypoalphalipoproteinemia
    n1=Goltz (syndrome de) | n2=en:hypoalphalipoproteinemia | rel=r_associated | relid=0 | w=27
  280. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:hypophosphatasia
    n1=Goltz (syndrome de) | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=27
  281. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ichthyosis
    n1=Goltz (syndrome de) | n2=en:ichthyosis | rel=r_associated | relid=0 | w=27
  282. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:in blood
    n1=Goltz (syndrome de) | n2=en:in blood | rel=r_associated | relid=0 | w=27
  283. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:intestinal atresia
    n1=Goltz (syndrome de) | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=27
  284. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:joubert syndrome
    n1=Goltz (syndrome de) | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=27
  285. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:kimura disease
    n1=Goltz (syndrome de) | n2=en:kimura disease | rel=r_associated | relid=0 | w=27
  286. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:lafora disease
    n1=Goltz (syndrome de) | n2=en:lafora disease | rel=r_associated | relid=0 | w=27
  287. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:linear or reticular hyperpigmentation
    n1=Goltz (syndrome de) | n2=en:linear or reticular hyperpigmentation | rel=r_associated | relid=0 | w=27
  288. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:lissencephaly
    n1=Goltz (syndrome de) | n2=en:lissencephaly | rel=r_associated | relid=0 | w=27
  289. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:majority of cases (95%) are sporadic
    n1=Goltz (syndrome de) | n2=en:majority of cases (95%) are sporadic | rel=r_associated | relid=0 | w=27
  290. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:malignant atrophic papulosis
    n1=Goltz (syndrome de) | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=27
  291. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:malocclusion
    n1=Goltz (syndrome de) | n2=en:malocclusion | rel=r_associated | relid=0 | w=27
  292. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:mental retardation, x-linked, snyder-robinson type
    n1=Goltz (syndrome de) | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=27
  293. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:mevalonate kinase deficiency
    n1=Goltz (syndrome de) | n2=en:mevalonate kinase deficiency | rel=r_associated | relid=0 | w=27
  294. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:monilethrix
    n1=Goltz (syndrome de) | n2=en:monilethrix | rel=r_associated | relid=0 | w=27
  295. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:mullerian inhibiting factor deficiency
    n1=Goltz (syndrome de) | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=27
  296. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:myhre syndrome
    n1=Goltz (syndrome de) | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=27
  297. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:myositis
    n1=Goltz (syndrome de) | n2=en:myositis | rel=r_associated | relid=0 | w=27
  298. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:myotonic disorder
    n1=Goltz (syndrome de) | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=27
  299. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:nelson syndrome
    n1=Goltz (syndrome de) | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=27
  300. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ninety percent of cases are female
    n1=Goltz (syndrome de) | n2=en:ninety percent of cases are female | rel=r_associated | relid=0 | w=27
  301. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:nursing therapy
    n1=Goltz (syndrome de) | n2=en:nursing therapy | rel=r_associated | relid=0 | w=27
  302. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:nutritional management
    n1=Goltz (syndrome de) | n2=en:nutritional management | rel=r_associated | relid=0 | w=27
  303. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ocular albinism type 1
    n1=Goltz (syndrome de) | n2=en:ocular albinism type 1 | rel=r_associated | relid=0 | w=27
  304. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:oesophageal papilloma
    n1=Goltz (syndrome de) | n2=en:oesophageal papilloma | rel=r_associated | relid=0 | w=27
  305. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=Goltz (syndrome de) | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=27
  306. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:omphalocele
    n1=Goltz (syndrome de) | n2=en:omphalocele | rel=r_associated | relid=0 | w=27
  307. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:orofaciodigital syndrome type 1
    n1=Goltz (syndrome de) | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=27
  308. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:pathological aspects
    n1=Goltz (syndrome de) | n2=en:pathological aspects | rel=r_associated | relid=0 | w=27
  309. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:phakomatosis
    n1=Goltz (syndrome de) | n2=en:phakomatosis | rel=r_associated | relid=0 | w=27
  310. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:porcn, arg365gln
    n1=Goltz (syndrome de) | n2=en:porcn, arg365gln | rel=r_associated | relid=0 | w=27
  311. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:port wine stain
    n1=Goltz (syndrome de) | n2=en:port wine stain | rel=r_associated | relid=0 | w=27
  312. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:potocki-lupski syndrome
    n1=Goltz (syndrome de) | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=27
  313. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:progressive bulbar palsy
    n1=Goltz (syndrome de) | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=27
  314. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:progressive supranuclear palsy
    n1=Goltz (syndrome de) | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=27
  315. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:rehabilitation aspects
    n1=Goltz (syndrome de) | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=27
  316. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:renpenning syndrome 1
    n1=Goltz (syndrome de) | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=27
  317. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:scleredema adultorum
    n1=Goltz (syndrome de) | n2=en:scleredema adultorum | rel=r_associated | relid=0 | w=27
  318. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:simpson golabi behmel syndrome type 1
    n1=Goltz (syndrome de) | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=27
  319. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:sjogren-larsson syndrome
    n1=Goltz (syndrome de) | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=27
  320. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:skin neoplasm
    n1=Goltz (syndrome de) | n2=en:skin neoplasm | rel=r_associated | relid=0 | w=27
  321. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:sparse hair
    n1=Goltz (syndrome de) | n2=en:sparse hair | rel=r_associated | relid=0 | w=27
  322. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:spondylocostal dysostosis 4, autosomal dominant
    n1=Goltz (syndrome de) | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=27
  323. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:sudden unexplained infant death
    n1=Goltz (syndrome de) | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=27
  324. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:syndactyly
    n1=Goltz (syndrome de) | n2=en:syndactyly | rel=r_associated | relid=0 | w=27
  325. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:tay-sachs disease
    n1=Goltz (syndrome de) | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=27
  326. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:thoracic outlet syndrome
    n1=Goltz (syndrome de) | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=27
  327. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:togaviridae infection
    n1=Goltz (syndrome de) | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=27
  328. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:tooth and nail syndrome
    n1=Goltz (syndrome de) | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=27
  329. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:tracheobronchomegaly
    n1=Goltz (syndrome de) | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=27
  330. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:umbilical hernia
    n1=Goltz (syndrome de) | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=27
  331. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:use of ultrasonography
    n1=Goltz (syndrome de) | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=27
  332. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:wegener granulomatosis
    n1=Goltz (syndrome de) | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=27
  333. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:x-linked bulbar-muscular atrophy
    n1=Goltz (syndrome de) | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=27
  334. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> en:x-linked dyskeratosis congenita
    n1=Goltz (syndrome de) | n2=en:x-linked dyskeratosis congenita | rel=r_associated | relid=0 | w=27
  335. Goltz (syndrome de) -- r_associated #0: 27 / 0.38 -> syndrome de goltz-gorlin
    n1=Goltz (syndrome de) | n2=syndrome de goltz-gorlin | rel=r_associated | relid=0 | w=27
  336. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:5 alpha steroid reductase 2 deficiency
    n1=Goltz (syndrome de) | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=26
  337. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:albinism
    n1=Goltz (syndrome de) | n2=en:albinism | rel=r_associated | relid=0 | w=26
  338. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
    n1=Goltz (syndrome de) | n2=en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections | rel=r_associated | relid=0 | w=26
  339. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:alstrom syndrome
    n1=Goltz (syndrome de) | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=26
  340. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:aortic coarctation
    n1=Goltz (syndrome de) | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=26
  341. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:arborescent papillomas (axillae, periumbilical area, anus, vulva)
    n1=Goltz (syndrome de) | n2=en:arborescent papillomas (axillae, periumbilical area, anus, vulva) | rel=r_associated | relid=0 | w=26
  342. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:autosomal dominant optic atrophy
    n1=Goltz (syndrome de) | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=26
  343. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:beare-stevenson cutis gyrata syndrome
    n1=Goltz (syndrome de) | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=26
  344. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:benign mucous membrane pemphigoid
    n1=Goltz (syndrome de) | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=26
  345. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:berardinelli-seip congenital lipodystrophy
    n1=Goltz (syndrome de) | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=26
  346. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:borjeson-forssman-lehmann syndrome
    n1=Goltz (syndrome de) | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=26
  347. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:cadasil syndrome
    n1=Goltz (syndrome de) | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=26
  348. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:camurati-engelmann syndrome
    n1=Goltz (syndrome de) | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=26
  349. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:carney complex
    n1=Goltz (syndrome de) | n2=en:carney complex | rel=r_associated | relid=0 | w=26
  350. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:cataplexy
    n1=Goltz (syndrome de) | n2=en:cataplexy | rel=r_associated | relid=0 | w=26
  351. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:chorea
    n1=Goltz (syndrome de) | n2=en:chorea | rel=r_associated | relid=0 | w=26
  352. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:choroideremia
    n1=Goltz (syndrome de) | n2=en:choroideremia | rel=r_associated | relid=0 | w=26
  353. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:cleft lip
    n1=Goltz (syndrome de) | n2=en:cleft lip | rel=r_associated | relid=0 | w=26
  354. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:cleidocranial dysplasia
    n1=Goltz (syndrome de) | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=26
  355. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:congenital erector pili hamartoma
    n1=Goltz (syndrome de) | n2=en:congenital erector pili hamartoma | rel=r_associated | relid=0 | w=26
  356. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:congenital melanocytic nevus
    n1=Goltz (syndrome de) | n2=en:congenital melanocytic nevus | rel=r_associated | relid=0 | w=26
  357. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:cryopyrin-associated periodic syndrome
    n1=Goltz (syndrome de) | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=26
  358. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:de sanctis-cacchione syndrome
    n1=Goltz (syndrome de) | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=26
  359. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:decreased visual acuity
    n1=Goltz (syndrome de) | n2=en:decreased visual acuity | rel=r_associated | relid=0 | w=26
  360. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:dentatorubral-pallidoluysian atrophy
    n1=Goltz (syndrome de) | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=26
  361. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:dermoids of cornea
    n1=Goltz (syndrome de) | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=26
  362. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:developmental dysplasia of hip
    n1=Goltz (syndrome de) | n2=en:developmental dysplasia of hip | rel=r_associated | relid=0 | w=26
  363. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:dextrocardia
    n1=Goltz (syndrome de) | n2=en:dextrocardia | rel=r_associated | relid=0 | w=26
  364. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:dyserythropoietic anemia with thrombocytopenia
    n1=Goltz (syndrome de) | n2=en:dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=26
  365. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:dystrophic nails (spooned, grooves)
    n1=Goltz (syndrome de) | n2=en:dystrophic nails (spooned, grooves) | rel=r_associated | relid=0 | w=26
  366. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:ebstein anomaly
    n1=Goltz (syndrome de) | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=26
  367. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:ectodermal dysplasia with natal teeth, turnpenny type
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=26
  368. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:ectodermal dysplasia with sweating defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with sweating defect | rel=r_associated | relid=0 | w=26
  369. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:emery-dreifuss muscular dystrophy
    n1=Goltz (syndrome de) | n2=en:emery-dreifuss muscular dystrophy | rel=r_associated | relid=0 | w=26
  370. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:enzymology
    n1=Goltz (syndrome de) | n2=en:enzymology | rel=r_associated | relid=0 | w=26
  371. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:epidermolysis bullosa
    n1=Goltz (syndrome de) | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=26
  372. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:external auditory canal narrow
    n1=Goltz (syndrome de) | n2=en:external auditory canal narrow | rel=r_associated | relid=0 | w=26
  373. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:familial dysautonomia
    n1=Goltz (syndrome de) | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=26
  374. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:farber lipogranulomatosis
    n1=Goltz (syndrome de) | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=26
  375. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:fraser syndrome
    n1=Goltz (syndrome de) | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=26
  376. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:fronto-naso-ethmoidal dysostosis
    n1=Goltz (syndrome de) | n2=en:fronto-naso-ethmoidal dysostosis | rel=r_associated | relid=0 | w=26
  377. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:genetic diseases, x-linked
    n1=Goltz (syndrome de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  378. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hemophagocytic lymphohistiocytosis
    n1=Goltz (syndrome de) | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=26
  379. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hemorrhagic fever with renal syndrome
    n1=Goltz (syndrome de) | n2=en:hemorrhagic fever with renal syndrome | rel=r_associated | relid=0 | w=26
  380. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hereditary angioedema
    n1=Goltz (syndrome de) | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=26
  381. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hidrocystoma
    n1=Goltz (syndrome de) | n2=en:hidrocystoma | rel=r_associated | relid=0 | w=26
  382. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:homocystinuria
    n1=Goltz (syndrome de) | n2=en:homocystinuria | rel=r_associated | relid=0 | w=26
  383. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hydrocephalus with cerebellar agenesis
    n1=Goltz (syndrome de) | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=26
  384. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:hypoplastic fingertip epidermal ridges
    n1=Goltz (syndrome de) | n2=en:hypoplastic fingertip epidermal ridges | rel=r_associated | relid=0 | w=26
  385. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:immunoglobulin a deficiency 1
    n1=Goltz (syndrome de) | n2=en:immunoglobulin a deficiency 1 | rel=r_associated | relid=0 | w=26
  386. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:jervell and lange nielsen syndrome
    n1=Goltz (syndrome de) | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=26
  387. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:kallmann syndrome
    n1=Goltz (syndrome de) | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=26
  388. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:klippel-feil syndrome
    n1=Goltz (syndrome de) | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=26
  389. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:klippel-trenaunay-weber syndrome
    n1=Goltz (syndrome de) | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=26
  390. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:lecithin acyltransferase deficiency
    n1=Goltz (syndrome de) | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=26
  391. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:machado-joseph disease
    n1=Goltz (syndrome de) | n2=en:machado-joseph disease | rel=r_associated | relid=0 | w=26
  392. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mallory-weiss syndrome
    n1=Goltz (syndrome de) | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=26
  393. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=Goltz (syndrome de) | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=26
  394. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mental retardation with psychosis, pyramidal signs, and macroorchidism
    n1=Goltz (syndrome de) | n2=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | rel=r_associated | relid=0 | w=26
  395. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mild microcephaly
    n1=Goltz (syndrome de) | n2=en:mild microcephaly | rel=r_associated | relid=0 | w=26
  396. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mitochondrial trifunctional protein deficiency
    n1=Goltz (syndrome de) | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=26
  397. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mobius syndrome
    n1=Goltz (syndrome de) | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=26
  398. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:mulibrey nanism
    n1=Goltz (syndrome de) | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=26
  399. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:muscular dystrophy
    n1=Goltz (syndrome de) | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=26
  400. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:neurotoxicity syndrome
    n1=Goltz (syndrome de) | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=26
  401. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:orofaciodigital syndrome type 6
    n1=Goltz (syndrome de) | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=26
  402. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:osteopathia striata
    n1=Goltz (syndrome de) | n2=en:osteopathia striata | rel=r_associated | relid=0 | w=26
  403. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:pachyonychia congenita
    n1=Goltz (syndrome de) | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=26
  404. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:pantothenate kinase-associated neurodegeneration
    n1=Goltz (syndrome de) | n2=en:pantothenate kinase-associated neurodegeneration | rel=r_associated | relid=0 | w=26
  405. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:panuveitis
    n1=Goltz (syndrome de) | n2=en:panuveitis | rel=r_associated | relid=0 | w=26
  406. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:parasitology
    n1=Goltz (syndrome de) | n2=en:parasitology | rel=r_associated | relid=0 | w=26
  407. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:paroxysmal extreme pain disorder
    n1=Goltz (syndrome de) | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=26
  408. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:perthes disease
    n1=Goltz (syndrome de) | n2=en:perthes disease | rel=r_associated | relid=0 | w=26
  409. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:pharmacotherapeutic
    n1=Goltz (syndrome de) | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=26
  410. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:physiopathological
    n1=Goltz (syndrome de) | n2=en:physiopathological | rel=r_associated | relid=0 | w=26
  411. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:pinta
    n1=Goltz (syndrome de) | n2=en:pinta | rel=r_associated | relid=0 | w=26
  412. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:piriformis muscle syndrome
    n1=Goltz (syndrome de) | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=26
  413. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:plummer-vinson syndrome
    n1=Goltz (syndrome de) | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=26
  414. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:porcn, trp74ter
    n1=Goltz (syndrome de) | n2=en:porcn, trp74ter | rel=r_associated | relid=0 | w=26
  415. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:rare non-neoplastic disorder
    n1=Goltz (syndrome de) | n2=en:rare non-neoplastic disorder | rel=r_associated | relid=0 | w=26
  416. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:regional abnormality of skin
    n1=Goltz (syndrome de) | n2=en:regional abnormality of skin | rel=r_associated | relid=0 | w=26
  417. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:robinow syndrome
    n1=Goltz (syndrome de) | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=26
  418. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:scimitar syndrome
    n1=Goltz (syndrome de) | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=26
  419. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:senter syndrome
    n1=Goltz (syndrome de) | n2=en:senter syndrome | rel=r_associated | relid=0 | w=26
  420. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:short metatarsal bones
    n1=Goltz (syndrome de) | n2=en:short metatarsal bones | rel=r_associated | relid=0 | w=26
  421. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:short stature homeobox deficiency
    n1=Goltz (syndrome de) | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=26
  422. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:skin diseases, genetic
    n1=Goltz (syndrome de) | n2=en:skin diseases, genetic | rel=r_associated | relid=0 | w=26
  423. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:specified anomalies of nails
    n1=Goltz (syndrome de) | n2=en:specified anomalies of nails | rel=r_associated | relid=0 | w=26
  424. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:spheno-frontal dysostosis
    n1=Goltz (syndrome de) | n2=en:spheno-frontal dysostosis | rel=r_associated | relid=0 | w=26
  425. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:spinal muscular atrophy
    n1=Goltz (syndrome de) | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=26
  426. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:spondyloepimetaphyseal dysplasia, sponastrime type
    n1=Goltz (syndrome de) | n2=en:spondyloepimetaphyseal dysplasia, sponastrime type | rel=r_associated | relid=0 | w=26
  427. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:stickler syndrome
    n1=Goltz (syndrome de) | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=26
  428. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:surgical aspects
    n1=Goltz (syndrome de) | n2=en:surgical aspects | rel=r_associated | relid=0 | w=26
  429. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:swyer james syndrome
    n1=Goltz (syndrome de) | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=26
  430. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:syringomyelia
    n1=Goltz (syndrome de) | n2=en:syringomyelia | rel=r_associated | relid=0 | w=26
  431. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:transient global amnesia
    n1=Goltz (syndrome de) | n2=en:transient global amnesia | rel=r_associated | relid=0 | w=26
  432. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:van der woude syndrome
    n1=Goltz (syndrome de) | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=26
  433. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
  434. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:x-linked dominant inheritance
    n1=Goltz (syndrome de) | n2=en:x-linked dominant inheritance | rel=r_associated | relid=0 | w=26
  435. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> en:x-linked dystonia parkinsonism
    n1=Goltz (syndrome de) | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=26
  436. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> hypoplasie
    n1=Goltz (syndrome de) | n2=hypoplasie | rel=r_associated | relid=0 | w=26
  437. Goltz (syndrome de) -- r_associated #0: 26 / 0.366 -> maladies
    n1=Goltz (syndrome de) | n2=maladies | rel=r_associated | relid=0 | w=26
  438. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:17q21 microdeletion syndrome
    n1=Goltz (syndrome de) | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=25
  439. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:22q telomere deletion syndrome
    n1=Goltz (syndrome de) | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=25
  440. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:acatalasemia
    n1=Goltz (syndrome de) | n2=en:acatalasemia | rel=r_associated | relid=0 | w=25
  441. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:achondrogenesis
    n1=Goltz (syndrome de) | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=25
  442. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=Goltz (syndrome de) | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=25
  443. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:anonychia of fingernails
    n1=Goltz (syndrome de) | n2=en:anonychia of fingernails | rel=r_associated | relid=0 | w=25
  444. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:arthrogryposis
    n1=Goltz (syndrome de) | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=25
  445. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:barth syndrome
    n1=Goltz (syndrome de) | n2=en:barth syndrome | rel=r_associated | relid=0 | w=25
  446. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:calciphylaxis
    n1=Goltz (syndrome de) | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=25
  447. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:carbohydrate-deficient glycoprotein syndrome
    n1=Goltz (syndrome de) | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=25
  448. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:cavernous lymphangioma of skin
    n1=Goltz (syndrome de) | n2=en:cavernous lymphangioma of skin | rel=r_associated | relid=0 | w=25
  449. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:chemically induced
    n1=Goltz (syndrome de) | n2=en:chemically induced | rel=r_associated | relid=0 | w=25
  450. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:congenital
    n1=Goltz (syndrome de) | n2=en:congenital | rel=r_associated | relid=0 | w=25
  451. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:congenital anomaly of subcutaneous tissue
    n1=Goltz (syndrome de) | n2=en:congenital anomaly of subcutaneous tissue | rel=r_associated | relid=0 | w=25
  452. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:congenital fiber-type disproportion
    n1=Goltz (syndrome de) | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=25
  453. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:congenital nephrogenic diabetes insipidus
    n1=Goltz (syndrome de) | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=25
  454. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:congenital structural myopathy
    n1=Goltz (syndrome de) | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=25
  455. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:connexin 26 gene anomaly
    n1=Goltz (syndrome de) | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=25
  456. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:craniofrontonasal dysplasia
    n1=Goltz (syndrome de) | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=25
  457. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:cryptophthalmos syndrome
    n1=Goltz (syndrome de) | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=25
  458. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:diffuse cerebral sclerosis of schilder
    n1=Goltz (syndrome de) | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=25
  459. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:duchenne muscular dystrophy
    n1=Goltz (syndrome de) | n2=en:duchenne muscular dystrophy | rel=r_associated | relid=0 | w=25
  460. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:factor v leiden
    n1=Goltz (syndrome de) | n2=en:factor v leiden | rel=r_associated | relid=0 | w=25
  461. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:familial mediterranean fever
    n1=Goltz (syndrome de) | n2=en:familial mediterranean fever | rel=r_associated | relid=0 | w=25
  462. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:familial periodic paralysis
    n1=Goltz (syndrome de) | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=25
  463. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:glycogen storage disease type vi
    n1=Goltz (syndrome de) | n2=en:glycogen storage disease type vi | rel=r_associated | relid=0 | w=25
  464. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:goodpasture syndrome
    n1=Goltz (syndrome de) | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=25
  465. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:griscelli syndrome type 2
    n1=Goltz (syndrome de) | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=25
  466. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:gyrate atrophy
    n1=Goltz (syndrome de) | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=25
  467. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:hartnup disease
    n1=Goltz (syndrome de) | n2=en:hartnup disease | rel=r_associated | relid=0 | w=25
  468. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:heritable pulmonary arterial hypertension
    n1=Goltz (syndrome de) | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=25
  469. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:hydroa vacciniforme
    n1=Goltz (syndrome de) | n2=en:hydroa vacciniforme | rel=r_associated | relid=0 | w=25
  470. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=Goltz (syndrome de) | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=25
  471. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:idiopathic hypersomnolence
    n1=Goltz (syndrome de) | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=25
  472. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:imperforate anus
    n1=Goltz (syndrome de) | n2=en:imperforate anus | rel=r_associated | relid=0 | w=25
  473. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:imperforate vagina
    n1=Goltz (syndrome de) | n2=en:imperforate vagina | rel=r_associated | relid=0 | w=25
  474. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:in cerebrospinal fluid
    n1=Goltz (syndrome de) | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=25
  475. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:inguinal hernia
    n1=Goltz (syndrome de) | n2=en:inguinal hernia | rel=r_associated | relid=0 | w=25
  476. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:intestinal malrotation
    n1=Goltz (syndrome de) | n2=en:intestinal malrotation | rel=r_associated | relid=0 | w=25
  477. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:kabuki syndrome
    n1=Goltz (syndrome de) | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=25
  478. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:lateral medullary syndrome
    n1=Goltz (syndrome de) | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=25
  479. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:leber hereditary optic atrophy
    n1=Goltz (syndrome de) | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=25
  480. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:lujan fryns syndrome
    n1=Goltz (syndrome de) | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=25
  481. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:malignant hyperthermia syndrome
    n1=Goltz (syndrome de) | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=25
  482. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:melas syndrome
    n1=Goltz (syndrome de) | n2=en:melas syndrome | rel=r_associated | relid=0 | w=25
  483. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:mental retardation, x-linked, syndromic, christianson type
    n1=Goltz (syndrome de) | n2=en:mental retardation, x-linked, syndromic, christianson type | rel=r_associated | relid=0 | w=25
  484. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:migrating partial seizures in infancy
    n1=Goltz (syndrome de) | n2=en:migrating partial seizures in infancy | rel=r_associated | relid=0 | w=25
  485. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:nadh dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:nadh dehydrogenase deficiency | rel=r_associated | relid=0 | w=25
  486. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:narrow nose
    n1=Goltz (syndrome de) | n2=en:narrow nose | rel=r_associated | relid=0 | w=25
  487. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:neurocysticercosis
    n1=Goltz (syndrome de) | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=25
  488. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:nevus comedonicus
    n1=Goltz (syndrome de) | n2=en:nevus comedonicus | rel=r_associated | relid=0 | w=25
  489. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:optic atrophy
    n1=Goltz (syndrome de) | n2=en:optic atrophy | rel=r_associated | relid=0 | w=25
  490. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:orofaciodigital syndromes
    n1=Goltz (syndrome de) | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=25
  491. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:osteopetrosis with renal tubular acidosis
    n1=Goltz (syndrome de) | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=25
  492. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:patchy alopecia (head, pubic area)
    n1=Goltz (syndrome de) | n2=en:patchy alopecia (head, pubic area) | rel=r_associated | relid=0 | w=25
  493. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:pelger-huet anomaly
    n1=Goltz (syndrome de) | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=25
  494. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:pelizaeus-merzbacher disease
    n1=Goltz (syndrome de) | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=25
  495. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:periventricular heterotopia, x-linked
    n1=Goltz (syndrome de) | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=25
  496. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:polydactyly
    n1=Goltz (syndrome de) | n2=en:polydactyly | rel=r_associated | relid=0 | w=25
  497. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:porokeratosis
    n1=Goltz (syndrome de) | n2=en:porokeratosis | rel=r_associated | relid=0 | w=25
  498. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:porokeratosis of mibelli
    n1=Goltz (syndrome de) | n2=en:porokeratosis of mibelli | rel=r_associated | relid=0 | w=25
  499. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:progeria
    n1=Goltz (syndrome de) | n2=en:progeria | rel=r_associated | relid=0 | w=25
  500. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:protruding, simple ears
    n1=Goltz (syndrome de) | n2=en:protruding, simple ears | rel=r_associated | relid=0 | w=25
  501. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:pseudohypoaldosteronism
    n1=Goltz (syndrome de) | n2=en:pseudohypoaldosteronism | rel=r_associated | relid=0 | w=25
  502. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:psychology qualifier
    n1=Goltz (syndrome de) | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=25
  503. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:pyruvate carboxylase deficiency
    n1=Goltz (syndrome de) | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=25
  504. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:rieger syndrome type 1
    n1=Goltz (syndrome de) | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=25
  505. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:russell-silver syndrome
    n1=Goltz (syndrome de) | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=25
  506. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:spina bifida occulta
    n1=Goltz (syndrome de) | n2=en:spina bifida occulta | rel=r_associated | relid=0 | w=25
  507. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:spondylocostal dysostosis
    n1=Goltz (syndrome de) | n2=en:spondylocostal dysostosis | rel=r_associated | relid=0 | w=25
  508. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:sunct syndrome
    n1=Goltz (syndrome de) | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=25
  509. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:transposition of great vessels
    n1=Goltz (syndrome de) | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=25
  510. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:trisomy 14 mosaicism
    n1=Goltz (syndrome de) | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=25
  511. Goltz (syndrome de) -- r_associated #0: 25 / 0.352 -> en:xxxy and xxxxy syndrome
    n1=Goltz (syndrome de) | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=25
  512. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:aagenaes syndrome
    n1=Goltz (syndrome de) | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=24
  513. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:abnormal dermatoglyphic pattern
    n1=Goltz (syndrome de) | n2=en:abnormal dermatoglyphic pattern | rel=r_associated | relid=0 | w=24
  514. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:acquired hyperostosis syndrome
    n1=Goltz (syndrome de) | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=24
  515. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:acrocallosal syndrome
    n1=Goltz (syndrome de) | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=24
  516. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=Goltz (syndrome de) | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=24
  517. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:alpha-methylacyl-coa racemase deficiency
    n1=Goltz (syndrome de) | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=24
  518. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:ameloonychohypohidrotic syndrome
    n1=Goltz (syndrome de) | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=24
  519. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:aplasia cutis congenita
    n1=Goltz (syndrome de) | n2=en:aplasia cutis congenita | rel=r_associated | relid=0 | w=24
  520. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:atrophoderma maculatum
    n1=Goltz (syndrome de) | n2=en:atrophoderma maculatum | rel=r_associated | relid=0 | w=24
  521. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:breasts asymmetrical
    n1=Goltz (syndrome de) | n2=en:breasts asymmetrical | rel=r_associated | relid=0 | w=24
  522. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:campomelic dysplasia
    n1=Goltz (syndrome de) | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=24
  523. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:cat-eye syndrome
    n1=Goltz (syndrome de) | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=24
  524. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:cerebrooculofacioskeletal syndrome
    n1=Goltz (syndrome de) | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=24
  525. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:chronic granulomatous disease
    n1=Goltz (syndrome de) | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=24
  526. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:clitoral hypoplasia
    n1=Goltz (syndrome de) | n2=en:clitoral hypoplasia | rel=r_associated | relid=0 | w=24
  527. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:coloboma of the iris
    n1=Goltz (syndrome de) | n2=en:coloboma of the iris | rel=r_associated | relid=0 | w=24
  528. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:congenital absence of soft tissue of distal phalanx of finger
    n1=Goltz (syndrome de) | n2=en:congenital absence of soft tissue of distal phalanx of finger | rel=r_associated | relid=0 | w=24
  529. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:congenital ectodermal dysplasia of face
    n1=Goltz (syndrome de) | n2=en:congenital ectodermal dysplasia of face | rel=r_associated | relid=0 | w=24
  530. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:cutis marmorata telangiectatica congenita
    n1=Goltz (syndrome de) | n2=en:cutis marmorata telangiectatica congenita | rel=r_associated | relid=0 | w=24
  531. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:ectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=24
  532. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:ectodermal dysplasia 3, anhidrotic
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia 3, anhidrotic | rel=r_associated | relid=0 | w=24
  533. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:enamel hypoplasia
    n1=Goltz (syndrome de) | n2=en:enamel hypoplasia | rel=r_associated | relid=0 | w=24
  534. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:exposure as collected domain
    n1=Goltz (syndrome de) | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=24
  535. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:failure of pubic bone fusion
    n1=Goltz (syndrome de) | n2=en:failure of pubic bone fusion | rel=r_associated | relid=0 | w=24
  536. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:feingold syndrome
    n1=Goltz (syndrome de) | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=24
  537. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:fetal akinesia deformation sequence
    n1=Goltz (syndrome de) | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=24
  538. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:fraxe intellectual disability syndrome
    n1=Goltz (syndrome de) | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=24
  539. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:fronto-frontal dysostosis
    n1=Goltz (syndrome de) | n2=en:fronto-frontal dysostosis | rel=r_associated | relid=0 | w=24
  540. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:glycine encephalopathy
    n1=Goltz (syndrome de) | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=24
  541. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:hepatolenticular degeneration
    n1=Goltz (syndrome de) | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=24
  542. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:hereditary edema of legs
    n1=Goltz (syndrome de) | n2=en:hereditary edema of legs | rel=r_associated | relid=0 | w=24
  543. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:high molecular weight kininogen deficiency
    n1=Goltz (syndrome de) | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=24
  544. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:holocarboxylase synthetase deficiency
    n1=Goltz (syndrome de) | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=24
  545. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=Goltz (syndrome de) | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=24
  546. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:horseshoe kidney
    n1=Goltz (syndrome de) | n2=en:horseshoe kidney | rel=r_associated | relid=0 | w=24
  547. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:hydronephrosis
    n1=Goltz (syndrome de) | n2=en:hydronephrosis | rel=r_associated | relid=0 | w=24
  548. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:hyperkalemic periodic paralysis
    n1=Goltz (syndrome de) | n2=en:hyperkalemic periodic paralysis | rel=r_associated | relid=0 | w=24
  549. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:hyperlysinemia
    n1=Goltz (syndrome de) | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=24
  550. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:immunodeficiency with hyper-igm type 2
    n1=Goltz (syndrome de) | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=24
  551. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:iridocorneal endothelial syndrome
    n1=Goltz (syndrome de) | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=24
  552. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:ischio-vertebral syndrome
    n1=Goltz (syndrome de) | n2=en:ischio-vertebral syndrome | rel=r_associated | relid=0 | w=24
  553. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:kartagener syndrome
    n1=Goltz (syndrome de) | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=24
  554. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:kleine-levin syndrome
    n1=Goltz (syndrome de) | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=24
  555. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:labial hypoplasia
    n1=Goltz (syndrome de) | n2=en:labial hypoplasia | rel=r_associated | relid=0 | w=24
  556. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:leigh disease
    n1=Goltz (syndrome de) | n2=en:leigh disease | rel=r_associated | relid=0 | w=24
  557. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:lig4 syndrome
    n1=Goltz (syndrome de) | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=24
  558. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:lipoid proteinosis of urbach and wiethe
    n1=Goltz (syndrome de) | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=24
  559. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:localized cutaneous deposits of superficial fat
    n1=Goltz (syndrome de) | n2=en:localized cutaneous deposits of superficial fat | rel=r_associated | relid=0 | w=24
  560. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:malakoplakia
    n1=Goltz (syndrome de) | n2=en:malakoplakia | rel=r_associated | relid=0 | w=24
  561. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:mental retardation (15%)
    n1=Goltz (syndrome de) | n2=en:mental retardation (15%) | rel=r_associated | relid=0 | w=24
  562. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:mental retardation, x-linked
    n1=Goltz (syndrome de) | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=24
  563. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:metabolic aspects
    n1=Goltz (syndrome de) | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=24
  564. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:midclavicular aplasia
    n1=Goltz (syndrome de) | n2=en:midclavicular aplasia | rel=r_associated | relid=0 | w=24
  565. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:moloney syndrome
    n1=Goltz (syndrome de) | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=24
  566. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=24
  567. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:nephrocalcinosis
    n1=Goltz (syndrome de) | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=24
  568. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:nephrogenic fibrosing dermopathy
    n1=Goltz (syndrome de) | n2=en:nephrogenic fibrosing dermopathy | rel=r_associated | relid=0 | w=24
  569. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:neural tube defect
    n1=Goltz (syndrome de) | n2=en:neural tube defect | rel=r_associated | relid=0 | w=24
  570. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:notched incisors
    n1=Goltz (syndrome de) | n2=en:notched incisors | rel=r_associated | relid=0 | w=24
  571. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:oculocerebrorenal syndrome
    n1=Goltz (syndrome de) | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=24
  572. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:oeis complex
    n1=Goltz (syndrome de) | n2=en:oeis complex | rel=r_associated | relid=0 | w=24
  573. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:orofacial cleft 1
    n1=Goltz (syndrome de) | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=24
  574. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:osteopoikilosis
    n1=Goltz (syndrome de) | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=24
  575. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:pallister-killian syndrome
    n1=Goltz (syndrome de) | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=24
  576. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:papillomas (lip, gingiva)
    n1=Goltz (syndrome de) | n2=en:papillomas (lip, gingiva) | rel=r_associated | relid=0 | w=24
  577. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:pentalogy of cantrell
    n1=Goltz (syndrome de) | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=24
  578. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:peters-plus syndrome
    n1=Goltz (syndrome de) | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=24
  579. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:piebaldism
    n1=Goltz (syndrome de) | n2=en:piebaldism | rel=r_associated | relid=0 | w=24
  580. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:pierre robin syndrome
    n1=Goltz (syndrome de) | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=24
  581. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:proteus syndrome
    n1=Goltz (syndrome de) | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=24
  582. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:pseudoachondroplasia
    n1=Goltz (syndrome de) | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=24
  583. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:pyruvate dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=24
  584. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:retinoschisis
    n1=Goltz (syndrome de) | n2=en:retinoschisis | rel=r_associated | relid=0 | w=24
  585. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:roberts syndrome
    n1=Goltz (syndrome de) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=24
  586. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:sclerema neonatorum
    n1=Goltz (syndrome de) | n2=en:sclerema neonatorum | rel=r_associated | relid=0 | w=24
  587. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:short metacarpal
    n1=Goltz (syndrome de) | n2=en:short metacarpal | rel=r_associated | relid=0 | w=24
  588. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:sotos syndrome
    n1=Goltz (syndrome de) | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=24
  589. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:spasmodic torticollis
    n1=Goltz (syndrome de) | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=24
  590. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:specified congenital anomalies of breast
    n1=Goltz (syndrome de) | n2=en:specified congenital anomalies of breast | rel=r_associated | relid=0 | w=24
  591. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:strabismus
    n1=Goltz (syndrome de) | n2=en:strabismus | rel=r_associated | relid=0 | w=24
  592. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:tolosa-hunt syndrome
    n1=Goltz (syndrome de) | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=24
  593. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:trichothiodystrophy
    n1=Goltz (syndrome de) | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=24
  594. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:trigger finger disorder
    n1=Goltz (syndrome de) | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=24
  595. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:variegate porphyria
    n1=Goltz (syndrome de) | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=24
  596. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:williams syndrome
    n1=Goltz (syndrome de) | n2=en:williams syndrome | rel=r_associated | relid=0 | w=24
  597. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:wolfram syndrome
    n1=Goltz (syndrome de) | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=24
  598. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:x-linked lissencephaly
    n1=Goltz (syndrome de) | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=24
  599. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:x-linked lymphoproliferative syndrome
    n1=Goltz (syndrome de) | n2=en:x-linked lymphoproliferative syndrome | rel=r_associated | relid=0 | w=24
  600. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> en:xerophthalmia
    n1=Goltz (syndrome de) | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=24
  601. Goltz (syndrome de) -- r_associated #0: 24 / 0.338 -> médecine
    (science)
    n1=Goltz (syndrome de) | n2=médecine
    (science)
    | rel=r_associated | relid=0 | w=24
  602. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> aires
    n1=Goltz (syndrome de) | n2=aires | rel=r_associated | relid=0 | w=23
  603. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:achenbach syndrome
    n1=Goltz (syndrome de) | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=23
  604. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:acromegaly
    n1=Goltz (syndrome de) | n2=en:acromegaly | rel=r_associated | relid=0 | w=23
  605. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:acute intermittent porphyria
    n1=Goltz (syndrome de) | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=23
  606. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:adiposis dolorosa
    n1=Goltz (syndrome de) | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=23
  607. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:albright's hereditary osteodystrophy
    n1=Goltz (syndrome de) | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=23
  608. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:amniotic band syndrome
    n1=Goltz (syndrome de) | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=23
  609. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:anencephaly
    n1=Goltz (syndrome de) | n2=en:anencephaly | rel=r_associated | relid=0 | w=23
  610. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:anteriorly placed anus
    n1=Goltz (syndrome de) | n2=en:anteriorly placed anus | rel=r_associated | relid=0 | w=23
  611. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:atrophic muscular disorder
    n1=Goltz (syndrome de) | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=23
  612. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:beta thalassemia x-linked thrombocytopenia syndrome
    n1=Goltz (syndrome de) | n2=en:beta thalassemia x-linked thrombocytopenia syndrome | rel=r_associated | relid=0 | w=23
  613. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:brunner syndrome
    n1=Goltz (syndrome de) | n2=en:brunner syndrome | rel=r_associated | relid=0 | w=23
  614. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:cardiofaciocutaneous syndrome
    n1=Goltz (syndrome de) | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=23
  615. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:cask related intellectual disability
    n1=Goltz (syndrome de) | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=23
  616. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:chromosome 2q37 deletion syndrome
    n1=Goltz (syndrome de) | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=23
  617. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:commissural lip pit
    n1=Goltz (syndrome de) | n2=en:commissural lip pit | rel=r_associated | relid=0 | w=23
  618. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:complex regional pain syndrome ii
    n1=Goltz (syndrome de) | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=23
  619. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:congenital abnormal synostosis
    n1=Goltz (syndrome de) | n2=en:congenital abnormal synostosis | rel=r_associated | relid=0 | w=23
  620. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:congenital bilateral aplasia of the vas deferens
    n1=Goltz (syndrome de) | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=23
  621. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:congenital skin disorder
    n1=Goltz (syndrome de) | n2=en:congenital skin disorder | rel=r_associated | relid=0 | w=23
  622. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:corpus callosum agenesis
    n1=Goltz (syndrome de) | n2=en:corpus callosum agenesis | rel=r_associated | relid=0 | w=23
  623. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:cutis laxa
    n1=Goltz (syndrome de) | n2=en:cutis laxa | rel=r_associated | relid=0 | w=23
  624. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:cystinuria
    n1=Goltz (syndrome de) | n2=en:cystinuria | rel=r_associated | relid=0 | w=23
  625. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:donohue syndrome
    n1=Goltz (syndrome de) | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=23
  626. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:duane syndrome
    n1=Goltz (syndrome de) | n2=en:duane syndrome | rel=r_associated | relid=0 | w=23
  627. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:dubowitz syndrome
    n1=Goltz (syndrome de) | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=23
  628. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:encephalocele
    n1=Goltz (syndrome de) | n2=en:encephalocele | rel=r_associated | relid=0 | w=23
  629. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:exfoliation syndrome
    n1=Goltz (syndrome de) | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=23
  630. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:familial juvenile nephronophthisis
    n1=Goltz (syndrome de) | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=23
  631. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=Goltz (syndrome de) | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=23
  632. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:fibromuscular dysplasia
    n1=Goltz (syndrome de) | n2=en:fibromuscular dysplasia | rel=r_associated | relid=0 | w=23
  633. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:giant axonal neuropathy
    n1=Goltz (syndrome de) | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=23
  634. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:gitelman syndrome
    n1=Goltz (syndrome de) | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=23
  635. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:glycogen storage disease
    n1=Goltz (syndrome de) | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=23
  636. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:gynatresia
    n1=Goltz (syndrome de) | n2=en:gynatresia | rel=r_associated | relid=0 | w=23
  637. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:hereditary benign intraepithelial dyskeratosis
    n1=Goltz (syndrome de) | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=23
  638. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:hereditary persistence of fetal hemoglobin
    n1=Goltz (syndrome de) | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=23
  639. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:holmes-adie syndrome
    n1=Goltz (syndrome de) | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=23
  640. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:hyperglycerolemia
    n1=Goltz (syndrome de) | n2=en:hyperglycerolemia | rel=r_associated | relid=0 | w=23
  641. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:hypoplasia
    n1=Goltz (syndrome de) | n2=en:hypoplasia | rel=r_associated | relid=0 | w=23
  642. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:idiopathic cd4-positive t-lymphocytopenia
    n1=Goltz (syndrome de) | n2=en:idiopathic cd4-positive t-lymphocytopenia | rel=r_associated | relid=0 | w=23
  643. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:immunology aspects
    n1=Goltz (syndrome de) | n2=en:immunology aspects | rel=r_associated | relid=0 | w=23
  644. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:in urine
    n1=Goltz (syndrome de) | n2=en:in urine | rel=r_associated | relid=0 | w=23
  645. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:isolated noncompaction of the ventricular myocardium
    n1=Goltz (syndrome de) | n2=en:isolated noncompaction of the ventricular myocardium | rel=r_associated | relid=0 | w=23
  646. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:joint laxity
    n1=Goltz (syndrome de) | n2=en:joint laxity | rel=r_associated | relid=0 | w=23
  647. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:juvenile x-linked retinoschisis
    n1=Goltz (syndrome de) | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=23
  648. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:kearns-sayre syndrome
    n1=Goltz (syndrome de) | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=23
  649. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:kluver-bucy syndrome
    n1=Goltz (syndrome de) | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=23
  650. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:kshv inflammatory cytokine syndrome
    n1=Goltz (syndrome de) | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=23
  651. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:late tooth eruption
    n1=Goltz (syndrome de) | n2=en:late tooth eruption | rel=r_associated | relid=0 | w=23
  652. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:leber congenital amaurosis
    n1=Goltz (syndrome de) | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=23
  653. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:lennox-gastaut syndrome
    n1=Goltz (syndrome de) | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=23
  654. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:lissencephaly, x-linked, 2
    n1=Goltz (syndrome de) | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=23
  655. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:marshall syndrome
    n1=Goltz (syndrome de) | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=23
  656. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:merrf syndrome
    n1=Goltz (syndrome de) | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=23
  657. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:microphthalmia, syndromic 1
    n1=Goltz (syndrome de) | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=23
  658. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:microphthalmia, syndromic 4 (disorder)
    n1=Goltz (syndrome de) | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=23
  659. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:mmih syndrome
    n1=Goltz (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
  660. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:neuroacanthocytosis
    n1=Goltz (syndrome de) | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=23
  661. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:neuropathy, hereditary sensory and autonomic, type vii
    n1=Goltz (syndrome de) | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=23
  662. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:osseous syndactyly of fingers - first web
    n1=Goltz (syndrome de) | n2=en:osseous syndactyly of fingers - first web | rel=r_associated | relid=0 | w=23
  663. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:other specified congenital malformations of integument
    n1=Goltz (syndrome de) | n2=en:other specified congenital malformations of integument | rel=r_associated | relid=0 | w=23
  664. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:other specified congenital malformations of skin
    n1=Goltz (syndrome de) | n2=en:other specified congenital malformations of skin | rel=r_associated | relid=0 | w=23
  665. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:paragonimiasis
    n1=Goltz (syndrome de) | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=23
  666. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:persistent fetal circulation
    n1=Goltz (syndrome de) | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=23
  667. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:pettigrew syndrome
    n1=Goltz (syndrome de) | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=23
  668. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:pointed chin
    n1=Goltz (syndrome de) | n2=en:pointed chin | rel=r_associated | relid=0 | w=23
  669. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:popliteal pterygium syndrome
    n1=Goltz (syndrome de) | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=23
  670. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:potocki-shaffer syndrome
    n1=Goltz (syndrome de) | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=23
  671. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:pseudohermaphroditism
    n1=Goltz (syndrome de) | n2=en:pseudohermaphroditism | rel=r_associated | relid=0 | w=23
  672. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:pseudotrisomy 13 syndrome
    n1=Goltz (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  673. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:pulmonary alveolar proteinosis
    n1=Goltz (syndrome de) | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=23
  674. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:radial aplasia-thrombocytopenia syndrome
    n1=Goltz (syndrome de) | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=23
  675. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:scleromyxedema
    n1=Goltz (syndrome de) | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=23
  676. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:stargardt disease
    n1=Goltz (syndrome de) | n2=en:stargardt disease | rel=r_associated | relid=0 | w=23
  677. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:status epilepticus
    n1=Goltz (syndrome de) | n2=en:status epilepticus | rel=r_associated | relid=0 | w=23
  678. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:surfactant protein deficiency
    n1=Goltz (syndrome de) | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=23
  679. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:tangier disease
    n1=Goltz (syndrome de) | n2=en:tangier disease | rel=r_associated | relid=0 | w=23
  680. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:telangiectasia
    n1=Goltz (syndrome de) | n2=en:telangiectasia | rel=r_associated | relid=0 | w=23
  681. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:thanatophoric dysplasia
    n1=Goltz (syndrome de) | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=23
  682. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:turcot syndrome
    n1=Goltz (syndrome de) | n2=en:turcot syndrome | rel=r_associated | relid=0 | w=23
  683. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:x-linked ichthyosis
    n1=Goltz (syndrome de) | n2=en:x-linked ichthyosis | rel=r_associated | relid=0 | w=23
  684. Goltz (syndrome de) -- r_associated #0: 23 / 0.324 -> en:xyy syndrome
    n1=Goltz (syndrome de) | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=23
  685. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:acrodermatitis
    n1=Goltz (syndrome de) | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=22
  686. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:acrofacial dysostosis
    n1=Goltz (syndrome de) | n2=en:acrofacial dysostosis | rel=r_associated | relid=0 | w=22
  687. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:adenine phosphoribosyltransferase deficiency
    n1=Goltz (syndrome de) | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=22
  688. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:anhidrotic ectodermal dysplasia 1
    n1=Goltz (syndrome de) | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=22
  689. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:asymmetrical skull
    n1=Goltz (syndrome de) | n2=en:asymmetrical skull | rel=r_associated | relid=0 | w=22
  690. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:bannayan syndrome
    n1=Goltz (syndrome de) | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=22
  691. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:brown-sequard syndrome
    n1=Goltz (syndrome de) | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=22
  692. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:carnitine palmitoyltransferase i deficiency
    n1=Goltz (syndrome de) | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=22
  693. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:cerebellar ataxia ectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=22
  694. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:cogan-reese syndrome
    n1=Goltz (syndrome de) | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=22
  695. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:congenital disorder of deglycosylation
    n1=Goltz (syndrome de) | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=22
  696. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:congenital epulis
    n1=Goltz (syndrome de) | n2=en:congenital epulis | rel=r_associated | relid=0 | w=22
  697. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:congenital hamartoma
    n1=Goltz (syndrome de) | n2=en:congenital hamartoma | rel=r_associated | relid=0 | w=22
  698. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:congenital hamartoma of skin
    n1=Goltz (syndrome de) | n2=en:congenital hamartoma of skin | rel=r_associated | relid=0 | w=22
  699. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:congenital pain insensitivity
    n1=Goltz (syndrome de) | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=22
  700. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:cutaneous lesion resulting from spina bifida
    n1=Goltz (syndrome de) | n2=en:cutaneous lesion resulting from spina bifida | rel=r_associated | relid=0 | w=22
  701. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:deafness, autosomal recessive 49
    n1=Goltz (syndrome de) | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=22
  702. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:diffuse idiopathic skeletal hyperostosis
    n1=Goltz (syndrome de) | n2=en:diffuse idiopathic skeletal hyperostosis | rel=r_associated | relid=0 | w=22
  703. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:dyggve-melchior-clausen syndrome
    n1=Goltz (syndrome de) | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=22
  704. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:ectodermal dysplasia with nail defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with nail defect | rel=r_associated | relid=0 | w=22
  705. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:empty sella syndrome
    n1=Goltz (syndrome de) | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=22
  706. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:fox-fordyce disease
    n1=Goltz (syndrome de) | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=22
  707. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:fragile x syndrome
    n1=Goltz (syndrome de) | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=22
  708. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:fryns syndrome
    n1=Goltz (syndrome de) | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=22
  709. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:fuchs endothelial dystrophy
    n1=Goltz (syndrome de) | n2=en:fuchs endothelial dystrophy | rel=r_associated | relid=0 | w=22
  710. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:gastroschisis
    n1=Goltz (syndrome de) | n2=en:gastroschisis | rel=r_associated | relid=0 | w=22
  711. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=Goltz (syndrome de) | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=22
  712. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hair-nail ectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:hair-nail ectodermal dysplasia | rel=r_associated | relid=0 | w=22
  713. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hajdu-cheney syndrome
    n1=Goltz (syndrome de) | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=22
  714. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hantavirus pulmonary syndrome
    n1=Goltz (syndrome de) | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=22
  715. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hemophilia a
    n1=Goltz (syndrome de) | n2=en:hemophilia a | rel=r_associated | relid=0 | w=22
  716. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hermansky-pudlak syndrome
    n1=Goltz (syndrome de) | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=22
  717. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hiatal hernia
    n1=Goltz (syndrome de) | n2=en:hiatal hernia | rel=r_associated | relid=0 | w=22
  718. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hmg-coa lyase deficiency
    n1=Goltz (syndrome de) | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=22
  719. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:holoprosencephaly
    n1=Goltz (syndrome de) | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=22
  720. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hunter syndrome
    n1=Goltz (syndrome de) | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=22
  721. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hypoplasia of nipple
    n1=Goltz (syndrome de) | n2=en:hypoplasia of nipple | rel=r_associated | relid=0 | w=22
  722. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:hypoplastic finger
    n1=Goltz (syndrome de) | n2=en:hypoplastic finger | rel=r_associated | relid=0 | w=22
  723. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:jeune syndrome
    n1=Goltz (syndrome de) | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=22
  724. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:kernicterus
    n1=Goltz (syndrome de) | n2=en:kernicterus | rel=r_associated | relid=0 | w=22
  725. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:kniest dysplasia
    n1=Goltz (syndrome de) | n2=en:kniest dysplasia | rel=r_associated | relid=0 | w=22
  726. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=Goltz (syndrome de) | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=22
  727. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:microcephaly microcornea syndrome seemanova type
    n1=Goltz (syndrome de) | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=22
  728. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:midclavicular hypoplasia
    n1=Goltz (syndrome de) | n2=en:midclavicular hypoplasia | rel=r_associated | relid=0 | w=22
  729. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:moyamoya disease
    n1=Goltz (syndrome de) | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=22
  730. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:muenke syndrome
    n1=Goltz (syndrome de) | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=22
  731. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:multicentric osteolysis, nodulosis, and arthropathy
    n1=Goltz (syndrome de) | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=22
  732. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:multiple system atrophy
    n1=Goltz (syndrome de) | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=22
  733. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:nance-horan syndrome
    n1=Goltz (syndrome de) | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=22
  734. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:ochronosis
    n1=Goltz (syndrome de) | n2=en:ochronosis | rel=r_associated | relid=0 | w=22
  735. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:olivopontocerebellar atrophy
    n1=Goltz (syndrome de) | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=22
  736. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:ornithine carbamoyltransferase deficiency disease
    n1=Goltz (syndrome de) | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=22
  737. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:ossification of posterior longitudinal ligament
    n1=Goltz (syndrome de) | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=22
  738. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:pain agnosia
    n1=Goltz (syndrome de) | n2=en:pain agnosia | rel=r_associated | relid=0 | w=22
  739. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:pallister-hall syndrome
    n1=Goltz (syndrome de) | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=22
  740. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:porcn, arg124ter
    n1=Goltz (syndrome de) | n2=en:porcn, arg124ter | rel=r_associated | relid=0 | w=22
  741. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:prolidase deficiency
    n1=Goltz (syndrome de) | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=22
  742. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:rhizomelic dysplasia
    n1=Goltz (syndrome de) | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=22
  743. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:roentgenographic
    n1=Goltz (syndrome de) | n2=en:roentgenographic | rel=r_associated | relid=0 | w=22
  744. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:rothmund-thomson syndrome
    n1=Goltz (syndrome de) | n2=en:rothmund-thomson syndrome | rel=r_associated | relid=0 | w=22
  745. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:short phalanx of finger
    n1=Goltz (syndrome de) | n2=en:short phalanx of finger | rel=r_associated | relid=0 | w=22
  746. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:short rib-polydactyly syndrome
    n1=Goltz (syndrome de) | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=22
  747. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:shprintzen-goldberg craniosynostosis syndrome
    n1=Goltz (syndrome de) | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=22
  748. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:smith-magenis syndrome
    n1=Goltz (syndrome de) | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=22
  749. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:staphylococcal scalded skin syndrome
    n1=Goltz (syndrome de) | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=22
  750. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:sturge-weber syndrome
    n1=Goltz (syndrome de) | n2=en:sturge-weber syndrome | rel=r_associated | relid=0 | w=22
  751. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:synpolydactyly
    n1=Goltz (syndrome de) | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=22
  752. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:thrombocytopenia 2
    n1=Goltz (syndrome de) | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=22
  753. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:tracheobronchomalacia
    n1=Goltz (syndrome de) | n2=en:tracheobronchomalacia | rel=r_associated | relid=0 | w=22
  754. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:trichorhinophalangeal syndrome type ii
    n1=Goltz (syndrome de) | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=22
  755. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:usher syndrome
    n1=Goltz (syndrome de) | n2=en:usher syndrome | rel=r_associated | relid=0 | w=22
  756. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:vitelliform macular dystrophy
    n1=Goltz (syndrome de) | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=22
  757. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:weaver syndrome
    n1=Goltz (syndrome de) | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=22
  758. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:webbed penis
    n1=Goltz (syndrome de) | n2=en:webbed penis | rel=r_associated | relid=0 | w=22
  759. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> en:wiskott-aldrich syndrome
    n1=Goltz (syndrome de) | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=22
  760. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> génodermatose
    n1=Goltz (syndrome de) | n2=génodermatose | rel=r_associated | relid=0 | w=22
  761. Goltz (syndrome de) -- r_associated #0: 22 / 0.31 -> processus pathologique
    n1=Goltz (syndrome de) | n2=processus pathologique | rel=r_associated | relid=0 | w=22
  762. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> (syndrome de)
    n1=Goltz (syndrome de) | n2=(syndrome de) | rel=r_associated | relid=0 | w=21
  763. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> Blaschko (lignes de)
    n1=Goltz (syndrome de) | n2=Blaschko (lignes de) | rel=r_associated | relid=0 | w=21
  764. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:abnormality of skin morphology
    n1=Goltz (syndrome de) | n2=en:abnormality of skin morphology | rel=r_associated | relid=0 | w=21
  765. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:accessory nipple
    n1=Goltz (syndrome de) | n2=en:accessory nipple | rel=r_associated | relid=0 | w=21
  766. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:achard syndrome
    n1=Goltz (syndrome de) | n2=en:achard syndrome | rel=r_associated | relid=0 | w=21
  767. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:acrodysostosis
    n1=Goltz (syndrome de) | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=21
  768. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:alopecia epilepsy oligophrenia syndrome of moynahan
    n1=Goltz (syndrome de) | n2=en:alopecia epilepsy oligophrenia syndrome of moynahan | rel=r_associated | relid=0 | w=21
  769. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:angiokeratoma corporis diffusum
    n1=Goltz (syndrome de) | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=21
  770. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:antithrombin iii deficiency
    n1=Goltz (syndrome de) | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=21
  771. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:aspects of radionuclide imaging
    n1=Goltz (syndrome de) | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=21
  772. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:ataxia, fatal x-linked, with deafness and loss of vision
    n1=Goltz (syndrome de) | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=21
  773. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:atransferrinemia
    n1=Goltz (syndrome de) | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=21
  774. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:auditory perceptual disorder
    n1=Goltz (syndrome de) | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=21
  775. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:autosomal recessive hypohidrotic ectodermal dysplasia
    n1=Goltz (syndrome de) | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=21
  776. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:bifid ureter
    n1=Goltz (syndrome de) | n2=en:bifid ureter | rel=r_associated | relid=0 | w=21
  777. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:brain iron accumulation type i syndrome
    n1=Goltz (syndrome de) | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=21
  778. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:brittle hair
    n1=Goltz (syndrome de) | n2=en:brittle hair | rel=r_associated | relid=0 | w=21
  779. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:carnosinemia
    n1=Goltz (syndrome de) | n2=en:carnosinemia | rel=r_associated | relid=0 | w=21
  780. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001)
    n1=Goltz (syndrome de) | n2=en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001) | rel=r_associated | relid=0 | w=21
  781. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cerebrotendinous xanthomatosis
    n1=Goltz (syndrome de) | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=21
  782. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=Goltz (syndrome de) | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=21
  783. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cleft palate
    n1=Goltz (syndrome de) | n2=en:cleft palate | rel=r_associated | relid=0 | w=21
  784. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:coloboma of the retina
    n1=Goltz (syndrome de) | n2=en:coloboma of the retina | rel=r_associated | relid=0 | w=21
  785. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:complex regional pain syndrome i
    n1=Goltz (syndrome de) | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=21
  786. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:congenital anomaly of epidermal appendages
    n1=Goltz (syndrome de) | n2=en:congenital anomaly of epidermal appendages | rel=r_associated | relid=0 | w=21
  787. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:congenital anomaly of nail
    n1=Goltz (syndrome de) | n2=en:congenital anomaly of nail | rel=r_associated | relid=0 | w=21
  788. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:congenital dyserythropoietic anemia
    n1=Goltz (syndrome de) | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=21
  789. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:congenital oculocutaneous hypopigmentation
    n1=Goltz (syndrome de) | n2=en:congenital oculocutaneous hypopigmentation | rel=r_associated | relid=0 | w=21
  790. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:craniosynostosis
    n1=Goltz (syndrome de) | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=21
  791. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cutaneous mastocytosis
    n1=Goltz (syndrome de) | n2=en:cutaneous mastocytosis | rel=r_associated | relid=0 | w=21
  792. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cutaneous vascular malformation
    n1=Goltz (syndrome de) | n2=en:cutaneous vascular malformation | rel=r_associated | relid=0 | w=21
  793. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:cytochrome-c oxidase deficiency
    n1=Goltz (syndrome de) | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=21
  794. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:dandy-walker malformation
    n1=Goltz (syndrome de) | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=21
  795. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:deafness, autosomal recessive 28
    n1=Goltz (syndrome de) | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=21
  796. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:deletion 18q syndrome
    n1=Goltz (syndrome de) | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=21
  797. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:diaphragmatic hernia
    n1=Goltz (syndrome de) | n2=en:diaphragmatic hernia | rel=r_associated | relid=0 | w=21
  798. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:dysostosis of bone of skull
    n1=Goltz (syndrome de) | n2=en:dysostosis of bone of skull | rel=r_associated | relid=0 | w=21
  799. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:ectodermal dysplasia with tooth-nail-sweating defect
    n1=Goltz (syndrome de) | n2=en:ectodermal dysplasia with tooth-nail-sweating defect | rel=r_associated | relid=0 | w=21
  800. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:ectromelia
    n1=Goltz (syndrome de) | n2=en:ectromelia | rel=r_associated | relid=0 | w=21
  801. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:ehlers-danlos syndrome
    n1=Goltz (syndrome de) | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=21
  802. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:episodic pain syndrome, familial, 3
    n1=Goltz (syndrome de) | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=21
  803. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:erythropoietic protoporphyria
    n1=Goltz (syndrome de) | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=21
  804. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:facial asymmetry
    n1=Goltz (syndrome de) | n2=en:facial asymmetry | rel=r_associated | relid=0 | w=21
  805. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:familial partial lipodystrophy
    n1=Goltz (syndrome de) | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=21
  806. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:friedreich ataxia
    n1=Goltz (syndrome de) | n2=en:friedreich ataxia | rel=r_associated | relid=0 | w=21
  807. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:gardner syndrome
    n1=Goltz (syndrome de) | n2=en:gardner syndrome | rel=r_associated | relid=0 | w=21
  808. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:generalized arterial calcification of infancy 1
    n1=Goltz (syndrome de) | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=21
  809. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:glucose-6-phosphate dehydrogenase deficiency anemia
    n1=Goltz (syndrome de) | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=21
  810. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hereditary fructose intolerance
    n1=Goltz (syndrome de) | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=21
  811. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hereditary hyperbilirubinemia
    n1=Goltz (syndrome de) | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=21
  812. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hereditary orotic aciduria
    n1=Goltz (syndrome de) | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=21
  813. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:historical aspects qualifier
    n1=Goltz (syndrome de) | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=21
  814. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hyaline membrane syndrome
    n1=Goltz (syndrome de) | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=21
  815. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hydrops fetalis
    n1=Goltz (syndrome de) | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=21
  816. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hymenolepiasis
    n1=Goltz (syndrome de) | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=21
  817. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:hypodontia
    n1=Goltz (syndrome de) | n2=en:hypodontia | rel=r_associated | relid=0 | w=21
  818. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:incontinentia pigmenti
    n1=Goltz (syndrome de) | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=21
  819. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:inherited cutis laxa
    n1=Goltz (syndrome de) | n2=en:inherited cutis laxa | rel=r_associated | relid=0 | w=21
  820. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:jackson-weiss syndrome
    n1=Goltz (syndrome de) | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=21
  821. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:korsakoff syndrome
    n1=Goltz (syndrome de) | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=21
  822. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:localized skin lesion
    n1=Goltz (syndrome de) | n2=en:localized skin lesion | rel=r_associated | relid=0 | w=21
  823. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:lysinuric protein intolerance
    n1=Goltz (syndrome de) | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=21
  824. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:marfan syndrome
    n1=Goltz (syndrome de) | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=21
  825. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:melorheostosis
    n1=Goltz (syndrome de) | n2=en:melorheostosis | rel=r_associated | relid=0 | w=21
  826. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:methylmalonic acidemia
    n1=Goltz (syndrome de) | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=21
  827. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:microbiological
    n1=Goltz (syndrome de) | n2=en:microbiological | rel=r_associated | relid=0 | w=21
  828. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=Goltz (syndrome de) | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=21
  829. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:microphthalmia (15%)
    n1=Goltz (syndrome de) | n2=en:microphthalmia (15%) | rel=r_associated | relid=0 | w=21
  830. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:mitochondrial neurogastrointestingal encephalopathy
    n1=Goltz (syndrome de) | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=21
  831. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:mixed hearing loss
    n1=Goltz (syndrome de) | n2=en:mixed hearing loss | rel=r_associated | relid=0 | w=21
  832. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:mowat-wilson syndrome
    n1=Goltz (syndrome de) | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=21
  833. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:neurocutaneous melanosis sequence
    n1=Goltz (syndrome de) | n2=en:neurocutaneous melanosis sequence | rel=r_associated | relid=0 | w=21
  834. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:non-trisomic autosomal aneuploidy
    n1=Goltz (syndrome de) | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=21
  835. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:papillon-lefevre syndrome
    n1=Goltz (syndrome de) | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=21
  836. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:pick's disease
    n1=Goltz (syndrome de) | n2=en:pick's disease | rel=r_associated | relid=0 | w=21
  837. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:placental steroid sulfatase deficiency
    n1=Goltz (syndrome de) | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=21
  838. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:plague
    n1=Goltz (syndrome de) | n2=en:plague | rel=r_associated | relid=0 | w=21
  839. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:preauricular dimple
    n1=Goltz (syndrome de) | n2=en:preauricular dimple | rel=r_associated | relid=0 | w=21
  840. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:primary hypertrophic osteoarthropathy
    n1=Goltz (syndrome de) | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=21
  841. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:primary progressive aphasia
    n1=Goltz (syndrome de) | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=21
  842. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:prune belly syndrome
    n1=Goltz (syndrome de) | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=21
  843. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:rubinstein-taybi syndrome
    n1=Goltz (syndrome de) | n2=en:rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=21
  844. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:schinzel-giedion midface-retraction syndrome
    n1=Goltz (syndrome de) | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=21
  845. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:skeletal asymmetry
    n1=Goltz (syndrome de) | n2=en:skeletal asymmetry | rel=r_associated | relid=0 | w=21
  846. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:specified anomalies of hair
    n1=Goltz (syndrome de) | n2=en:specified anomalies of hair | rel=r_associated | relid=0 | w=21
  847. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:spondyloepimetaphyseal dysplasia with joint laxity type 2
    n1=Goltz (syndrome de) | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=21
  848. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:stiff person syndrome
    n1=Goltz (syndrome de) | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=21
  849. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:superior mesenteric artery syndrome
    n1=Goltz (syndrome de) | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=21
  850. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:synophrys
    n1=Goltz (syndrome de) | n2=en:synophrys | rel=r_associated | relid=0 | w=21
  851. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:thyroid hormone resistance syndrome
    n1=Goltz (syndrome de) | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=21
  852. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:trichinosis
    n1=Goltz (syndrome de) | n2=en:trichinosis | rel=r_associated | relid=0 | w=21
  853. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:trichorhinophalangeal syndrome type i
    n1=Goltz (syndrome de) | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=21
  854. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:turner syndrome
    n1=Goltz (syndrome de) | n2=en:turner syndrome | rel=r_associated | relid=0 | w=21
  855. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:urea cycle metabolism disorder
    n1=Goltz (syndrome de) | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=21
  856. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:veterinary aspects
    n1=Goltz (syndrome de) | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=21
  857. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:waardenburg syndrome
    n1=Goltz (syndrome de) | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=21
  858. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:waterhouse-friderichsen syndrome
    n1=Goltz (syndrome de) | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=21
  859. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:weill-marchesani syndrome
    n1=Goltz (syndrome de) | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=21
  860. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:west syndrome
    n1=Goltz (syndrome de) | n2=en:west syndrome | rel=r_associated | relid=0 | w=21
  861. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:x-linked agammaglobulinemia
    n1=Goltz (syndrome de) | n2=en:x-linked agammaglobulinemia | rel=r_associated | relid=0 | w=21
  862. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:x-linked dominant hypophosphatemic rickets
    n1=Goltz (syndrome de) | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=21
  863. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> en:x-linked epilepsy with learning disability and behavior disorder syndrome
    n1=Goltz (syndrome de) | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=21
  864. Goltz (syndrome de) -- r_associated #0: 21 / 0.296 -> syndrome de Goltz
    n1=Goltz (syndrome de) | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=21
  865. Goltz (syndrome de) -- r_associated #0: 20 / 0.282 -> en:angiolipomatous hamartoma
    n1=Goltz (syndrome de) | n2=en:angiolipomatous hamartoma | rel=r_associated | relid=0 | w=20
  866. Goltz (syndrome de) -- r_associated #0: 20 / 0.282 -> en:nævus angiolipomatosus
    n1=Goltz (syndrome de) | n2=en:nævus angiolipomatosus | rel=r_associated | relid=0 | w=20
  867. Goltz (syndrome de) -- r_associated #0: 20 / 0.282 -> en:Voorhoeve syndrome
    n1=Goltz (syndrome de) | n2=en:Voorhoeve syndrome | rel=r_associated | relid=0 | w=20
  868. Goltz (syndrome de) -- r_associated #0: 15 / 0.211 -> dysplasie dermique focale
    n1=Goltz (syndrome de) | n2=dysplasie dermique focale | rel=r_associated | relid=0 | w=15
  869. Goltz (syndrome de) -- r_associated #0: 15 / 0.211 -> syndrome de Goltz-Gorlin
    n1=Goltz (syndrome de) | n2=syndrome de Goltz-Gorlin | rel=r_associated | relid=0 | w=15
  870. Goltz (syndrome de) -- r_associated #0: 10 / 0.141 -> dysplasie dermique focale de Goltz
    n1=Goltz (syndrome de) | n2=dysplasie dermique focale de Goltz | rel=r_associated | relid=0 | w=10
  871. Goltz (syndrome de) -- r_associated #0: 10 / 0.141 -> en:Goltz syndrome
    n1=Goltz (syndrome de) | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=10
  872. Goltz (syndrome de) -- r_associated #0: 10 / 0.141 -> syndrome de goltz
    n1=Goltz (syndrome de) | n2=syndrome de goltz | rel=r_associated | relid=0 | w=10
≈ 553 relations entrantes

  1. syndrome de Goltz --- r_associated #0: 82 --> Goltz (syndrome de)
    n1=syndrome de Goltz | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=82
  2. hypoplasie dermique focale --- r_associated #0: 80 --> Goltz (syndrome de)
    n1=hypoplasie dermique focale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=80
  3. Goltz --- r_associated #0: 79 --> Goltz (syndrome de)
    n1=Goltz | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=79
  4. hypoplasie dermique en aires --- r_associated #0: 78 --> Goltz (syndrome de)
    n1=hypoplasie dermique en aires | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=78
  5. en:focal dermal hypoplasia --- r_associated #0: 77 --> Goltz (syndrome de)
    n1=en:focal dermal hypoplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=77
  6. (syndrome de) --- r_associated #0: 52 --> Goltz (syndrome de)
    n1=(syndrome de) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=52
  7. en:osteopathia striata --- r_associated #0: 40 --> Goltz (syndrome de)
    n1=en:osteopathia striata | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=40
  8. hamartome angiolipomateux de Howell --- r_associated #0: 40 --> Goltz (syndrome de)
    n1=hamartome angiolipomateux de Howell | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=40
  9. ostéopathie striée --- r_associated #0: 40 --> Goltz (syndrome de)
    n1=ostéopathie striée | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=40
  10. en:Voorhoeve syndrome --- r_associated #0: 38 --> Goltz (syndrome de)
    n1=en:Voorhoeve syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=38
  11. en:nævus angiolipomatosus --- r_associated #0: 36 --> Goltz (syndrome de)
    n1=en:nævus angiolipomatosus | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=36
  12. en:angiolipomatous hamartoma --- r_associated #0: 34 --> Goltz (syndrome de)
    n1=en:angiolipomatous hamartoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=34
  13. leucinose --- r_associated #0: 25 --> Goltz (syndrome de)
    n1=leucinose | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=25
  14. syndrome de goltz --- r_associated #0: 23 --> Goltz (syndrome de)
    n1=syndrome de goltz | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=23
  15. dermique --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=dermique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  16. dysplasie olfacto-génitale --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=dysplasie olfacto-génitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  17. dysplasie olfactogénitale --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=dysplasie olfactogénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  18. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=dysplasie olfactogénitale de De Morsier | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  19. déficit en phosphatases alcalines --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=déficit en phosphatases alcalines | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  20. en:1p36 deletion syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:1p36 deletion syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  21. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:5 alpha steroid reductase 2 deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  22. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  23. en:abetalipoproteinemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:abetalipoproteinemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  24. en:absence of toe --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:absence of toe | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  25. en:absent toenails --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:absent toenails | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  26. en:achromatopsia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:achromatopsia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  27. en:acrocephalosyndactyly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:acrocephalosyndactyly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  28. en:acrodermatitis enteropathica --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:acrodermatitis enteropathica | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  29. en:adolescent x-linked adrenoleukodystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:adolescent x-linked adrenoleukodystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  30. en:affected males are all result of new mutation --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:affected males are all result of new mutation | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  31. en:agnosia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:agnosia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  32. en:aicardi syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aicardi syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  33. en:ainhum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ainhum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  34. en:albinism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:albinism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  35. en:alkaptonuria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:alkaptonuria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  36. en:allan-herndon-dudley syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:allan-herndon-dudley syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  37. en:allgrove syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:allgrove syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  38. en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  39. en:alstrom syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:alstrom syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  40. en:amaurosis fugax --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:amaurosis fugax | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  41. en:analbuminemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:analbuminemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  42. en:andersen syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:andersen syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  43. en:androgen insensitivity syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:androgen insensitivity syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  44. en:anhydrotic ectodermal dysplasias --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:anhydrotic ectodermal dysplasias | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  45. en:aniridia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aniridia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  46. en:aniridia (3%) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aniridia (3%) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  47. en:anophthalmos --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:anophthalmos | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  48. en:aortic coarctation --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aortic coarctation | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  49. en:aprosencephaly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aprosencephaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  50. en:arakawa syndrome ii --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:arakawa syndrome ii | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  51. en:arborescent papillomas (axillae, periumbilical area, anus, vulva) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:arborescent papillomas (axillae, periumbilical area, anus, vulva) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  52. en:argininemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:argininemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  53. en:argininosuccinic aciduria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:argininosuccinic aciduria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  54. en:arnold-chiari malformation --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:arnold-chiari malformation | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  55. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:arrhythmogenic right ventricular dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  56. en:aspects of mortality statistics --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:aspects of mortality statistics | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  57. en:autoimmune polyendocrinopathy syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:autoimmune polyendocrinopathy syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  58. en:autosomal dominant optic atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:autosomal dominant optic atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  59. en:bartter syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:bartter syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  60. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:beare-stevenson cutis gyrata syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  61. en:benign mucous membrane pemphigoid --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:benign mucous membrane pemphigoid | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  62. en:berardinelli-seip congenital lipodystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:berardinelli-seip congenital lipodystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  63. en:bernard-soulier syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:bernard-soulier syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  64. en:beta-methylcrotonylglycinuria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:beta-methylcrotonylglycinuria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  65. en:biotinidase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:biotinidase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  66. en:birthmark --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:birthmark | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  67. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:borjeson-forssman-lehmann syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  68. en:brachydactyly (60%) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:brachydactyly (60%) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  69. en:broad nasal tip --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:broad nasal tip | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  70. en:brugsch's syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:brugsch's syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  71. en:cadasil syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cadasil syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  72. en:camurati-engelmann syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:camurati-engelmann syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  73. en:carney complex --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:carney complex | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  74. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  75. en:caroli disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:caroli disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  76. en:cartilage hair hypoplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cartilage hair hypoplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  77. en:cataplexy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cataplexy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  78. en:centrofacial lentiginosis syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:centrofacial lentiginosis syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  79. en:charge syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:charge syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  80. en:chilblains --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:chilblains | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  81. en:childhood cerebral x-linked adrenoleukodystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:childhood cerebral x-linked adrenoleukodystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  82. en:chondrodysplasia punctata --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:chondrodysplasia punctata | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  83. en:chorea --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:chorea | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  84. en:choroideremia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:choroideremia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  85. en:classical maple syrup urine disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:classical maple syrup urine disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  86. en:cleft ala nasi --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cleft ala nasi | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  87. en:cleft lip --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cleft lip | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  88. en:cleidocranial dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cleidocranial dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  89. en:codas syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:codas syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  90. en:coffin-lowry syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:coffin-lowry syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  91. en:combined lipase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:combined lipase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  92. en:complication aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:complication aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  93. en:congenital abnormality --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital abnormality | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  94. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  95. en:congenital anomaly of hair --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital anomaly of hair | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  96. en:congenital cortical hyperostosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital cortical hyperostosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  97. en:congenital erector pili hamartoma --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital erector pili hamartoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  98. en:congenital fecal fistula --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital fecal fistula | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  99. en:congenital hyperplasia of sebaceous glands of lip --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital hyperplasia of sebaceous glands of lip | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  100. en:congenital ichthyosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital ichthyosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  101. en:congenital insensitivity to pain with anhidrosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital insensitivity to pain with anhidrosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  102. en:congenital melanocytic nevus --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital melanocytic nevus | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  103. en:congenital myasthenic syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital myasthenic syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  104. en:congenital parameatal cyst --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital parameatal cyst | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  105. en:congenital phimosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital phimosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  106. en:congenital pigmentary skin anomalies --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital pigmentary skin anomalies | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  107. en:congenital scar --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:congenital scar | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  108. en:cor triatriatum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cor triatriatum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  109. en:cowden syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cowden syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  110. en:cranioectodermal dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cranioectodermal dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  111. en:craniofacial dysostosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:craniofacial dysostosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  112. en:cryopyrin-associated periodic syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cryopyrin-associated periodic syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  113. en:cutaneous lesion resulting from spinal dysraphism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cutaneous lesion resulting from spinal dysraphism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  114. en:cystathioninuria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:cystathioninuria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  115. en:d-bifunctional protein deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:d-bifunctional protein deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  116. en:d-glyceric aciduria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:d-glyceric aciduria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  117. en:darier disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:darier disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  118. en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:de sanctis-cacchione syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  119. en:deafness, autosomal recessive 1a --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:deafness, autosomal recessive 1a | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  120. en:decreased visual acuity --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:decreased visual acuity | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  121. en:deletion 18p syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:deletion 18p syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  122. en:dent's disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dent's disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  123. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dentatorubral-pallidoluysian atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  124. en:dentinogenesis imperfecta --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dentinogenesis imperfecta | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  125. en:dermal sinus --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dermal sinus | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  126. en:dermoids of cornea --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dermoids of cornea | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  127. en:developmental dysplasia of hip --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:developmental dysplasia of hip | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  128. en:dextrocardia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dextrocardia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  129. en:diagnosis aspect --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:diagnosis aspect | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  130. en:diastasis recti --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:diastasis recti | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  131. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  132. en:distichiasis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:distichiasis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  133. en:dmd-associated dilated cardiomyopathy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dmd-associated dilated cardiomyopathy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  134. en:double eyebrow --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:double eyebrow | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  135. en:drug- and toxin-induced pulmonary arterial hypertension --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  136. en:dyschromatosis symmetrica hereditaria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dyschromatosis symmetrica hereditaria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  137. en:dyserythropoietic anemia with thrombocytopenia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dyserythropoietic anemia with thrombocytopenia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  138. en:dyskeratosis congenita --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dyskeratosis congenita | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  139. en:dysostosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dysostosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  140. en:dysplastic cerebellar gangliocytoma --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dysplastic cerebellar gangliocytoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  141. en:dystrophic nails (spooned, grooves) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:dystrophic nails (spooned, grooves) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  142. en:ebstein anomaly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ebstein anomaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  143. en:ectodermal dysplasia with hair-nail defect --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with hair-nail defect | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  144. en:ectodermal dysplasia with hair-tooth defects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with hair-tooth defects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  145. en:ectodermal dysplasia with hair-tooth-nail defects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with hair-tooth-nail defects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  146. en:ectodermal dysplasia with hair-tooth-nail-sweating defect --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with hair-tooth-nail-sweating defect | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  147. en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  148. en:ectodermal dysplasia with sweating defect --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with sweating defect | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  149. en:ectodermal dysplasia with tooth-nail defects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with tooth-nail defects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  150. en:ectodermal dysplasia with tooth-sweating defect --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectodermal dysplasia with tooth-sweating defect | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  151. en:ectopia lentis (6%) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectopia lentis (6%) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  152. en:ectrodactyly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ectrodactyly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  153. en:ellis-van creveld syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ellis-van creveld syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  154. en:embryologic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:embryologic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  155. en:emery-dreifuss muscular dystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:emery-dreifuss muscular dystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  156. en:enzymology --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:enzymology | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  157. en:epidemiologic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:epidemiologic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  158. en:epidermodysplasia verruciformis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:epidermodysplasia verruciformis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  159. en:epidermolysis bullosa --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:epidermolysis bullosa | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  160. en:erythrokeratodermia variabilis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:erythrokeratodermia variabilis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  161. en:erythromelalgia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:erythromelalgia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  162. en:erythropoietic porphyria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:erythropoietic porphyria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  163. en:ethnologic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ethnologic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  164. en:etiology aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:etiology aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  165. en:external auditory canal narrow --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:external auditory canal narrow | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  166. en:familial dysautonomia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:familial dysautonomia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  167. en:familial hypertrophic cardiomyopathy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:familial hypertrophic cardiomyopathy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  168. en:farber lipogranulomatosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:farber lipogranulomatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  169. en:fatal familial insomnia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:fatal familial insomnia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  170. en:felty syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:felty syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  171. en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:fibrodysplasia ossificans progressiva | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  172. en:focal facial dermal dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:focal facial dermal dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  173. en:fraser syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:fraser syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  174. en:fronto-naso-ethmoidal dysostosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:fronto-naso-ethmoidal dysostosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  175. en:frontonasal dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:frontonasal dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  176. en:frontotemporal dementia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:frontotemporal dementia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  177. en:gangrenous stomatitis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:gangrenous stomatitis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  178. en:gastric antral vascular ectasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:gastric antral vascular ectasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  179. en:generalized abnormality of skin --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:generalized abnormality of skin | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  180. en:genetic aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:genetic aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  181. en:genetic diseases, x-linked --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:genetic diseases, x-linked | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  182. en:genitoperineal raphe cyst --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:genitoperineal raphe cyst | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  183. en:genu varum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:genu varum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  184. en:gerstmann-straussler-scheinker disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:gerstmann-straussler-scheinker disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  185. en:glanzmann thrombasthenia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:glanzmann thrombasthenia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  186. en:glutaric acidemia type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:glutaric acidemia type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  187. en:glycogen storage disease type iib --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:glycogen storage disease type iib | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  188. en:glycogen storage disease type viii --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:glycogen storage disease type viii | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  189. en:goldenhar syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:goldenhar syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  190. en:gray platelet syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:gray platelet syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  191. en:hallermann syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hallermann syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  192. en:hamartoma --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hamartoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  193. en:hard skin syndrome parana type --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hard skin syndrome parana type | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  194. en:hellp syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hellp syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  195. en:hemangiomatosis with thrombocytopenia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hemangiomatosis with thrombocytopenia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  196. en:hemochromatosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hemochromatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  197. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hemophagocytic lymphohistiocytosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  198. en:hemophilia b --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hemophilia b | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  199. en:hemorrhagic fever with renal syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hemorrhagic fever with renal syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  200. en:hereditary angioedema --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hereditary angioedema | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  201. en:hereditary coproporphyria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hereditary coproporphyria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  202. en:hereditary hemorrhagic telangiectasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hereditary hemorrhagic telangiectasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  203. en:hereditary mucosal leukokeratosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hereditary mucosal leukokeratosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  204. en:heterotaxy syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:heterotaxy syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  205. en:hidrocystoma --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hidrocystoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  206. en:hidrotic ectodermal dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hidrotic ectodermal dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  207. en:holt-oram syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:holt-oram syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  208. en:homocystinuria --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:homocystinuria | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  209. en:hooded penis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hooded penis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  210. en:hydrocephalus --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hydrocephalus | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  211. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hydrocephalus with cerebellar agenesis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  212. en:hyper-igm immunodeficiency syndrome, type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hyper-igm immunodeficiency syndrome, type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  213. en:hyperpipecolatemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hyperpipecolatemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  214. en:hypoalphalipoproteinemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hypoalphalipoproteinemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  215. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  216. en:hypokalemic periodic paralysis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hypokalemic periodic paralysis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  217. en:hypophosphatasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hypophosphatasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  218. en:hypoplastic fingertip epidermal ridges --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:hypoplastic fingertip epidermal ridges | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  219. en:ichthyosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ichthyosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  220. en:immunoglobulin a deficiency 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:immunoglobulin a deficiency 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  221. en:in blood --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:in blood | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  222. en:infantile neuroaxonal dystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:infantile neuroaxonal dystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  223. en:intestinal atresia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:intestinal atresia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  224. en:jacobsen syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:jacobsen syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  225. en:jervell and lange nielsen syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:jervell and lange nielsen syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  226. en:joubert syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:joubert syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  227. en:kallmann syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:kallmann syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  228. en:kimura disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:kimura disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  229. en:kirman syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:kirman syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  230. en:klippel-feil syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:klippel-feil syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  231. en:klippel-trenaunay-weber syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:klippel-trenaunay-weber syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  232. en:lafora disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lafora disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  233. en:landau-kleffner syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:landau-kleffner syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  234. en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lecithin acyltransferase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  235. en:leopard syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:leopard syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  236. en:leprosy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:leprosy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  237. en:leptospirosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:leptospirosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  238. en:leri-weill dyschondrosteosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:leri-weill dyschondrosteosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  239. en:lesch-nyhan syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lesch-nyhan syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  240. en:leukodystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:leukodystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  241. en:levocardia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:levocardia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  242. en:liddle syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:liddle syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  243. en:linear or reticular hyperpigmentation --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:linear or reticular hyperpigmentation | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  244. en:lissencephaly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lissencephaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  245. en:loeys-dietz syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:loeys-dietz syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  246. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  247. en:low set ears --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:low set ears | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  248. en:lubs x-linked mental retardation syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lubs x-linked mental retardation syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  249. en:lumpy scalp syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lumpy scalp syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  250. en:lysosomal storage disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:lysosomal storage disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  251. en:machado-joseph disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:machado-joseph disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  252. en:maffucci syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:maffucci syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  253. en:majority of cases (95%) are sporadic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:majority of cases (95%) are sporadic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  254. en:malformations of cortical development --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:malformations of cortical development | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  255. en:malignant atrophic papulosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:malignant atrophic papulosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  256. en:mallory-weiss syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mallory-weiss syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  257. en:malocclusion --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:malocclusion | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  258. en:mansonelliasis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mansonelliasis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  259. en:maple syrup urine disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:maple syrup urine disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  260. en:marburg virus disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:marburg virus disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  261. en:masa syndrome (disorder) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:masa syndrome (disorder) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  262. en:mayer-rokitansky-kuster-hauser syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  263. en:meckel-gruber syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:meckel-gruber syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  264. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  265. en:meesmann corneal dystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:meesmann corneal dystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  266. en:melkersson-rosenthal syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:melkersson-rosenthal syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  267. en:meningeal tuberculosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:meningeal tuberculosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  268. en:menkes disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:menkes disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  269. en:mental retardation with psychosis, pyramidal signs, and macroorchidism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  270. en:mental retardation, x-linked, snyder-robinson type --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mental retardation, x-linked, snyder-robinson type | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  271. en:methionine adenosyltransferase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:methionine adenosyltransferase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  272. en:mevalonate kinase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mevalonate kinase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  273. en:microphthalmia, syndromic 2 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:microphthalmia, syndromic 2 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  274. en:mild microcephaly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mild microcephaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  275. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mitochondrial trifunctional protein deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  276. en:mixed connective tissue disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mixed connective tissue disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  277. en:mobius syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mobius syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  278. en:mohr-tranebjaerg syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mohr-tranebjaerg syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  279. en:molybdenum cofactor deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:molybdenum cofactor deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  280. en:monilethrix --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:monilethrix | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  281. en:mulibrey nanism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mulibrey nanism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  282. en:mullerian inhibiting factor deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:mullerian inhibiting factor deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  283. en:muscular dystrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:muscular dystrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  284. en:myelomeningocele --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:myelomeningocele | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  285. en:myhre syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:myhre syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  286. en:myokymia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:myokymia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  287. en:myositis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:myositis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  288. en:myotonic disorder --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:myotonic disorder | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  289. en:n-acetylglutamate synthase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:n-acetylglutamate synthase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  290. en:nail-patella syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:nail-patella syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  291. en:nelson syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:nelson syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  292. en:neonatal progeroid syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:neonatal progeroid syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  293. en:neuromyelitis optica --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:neuromyelitis optica | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  294. en:neuronal intranuclear inclusion disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:neuronal intranuclear inclusion disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  295. en:neurotoxicity syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:neurotoxicity syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  296. en:ninety percent of cases are female --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ninety percent of cases are female | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  297. en:norrie syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:norrie syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  298. en:nursing therapy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:nursing therapy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  299. en:nutritional management --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:nutritional management | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  300. en:nystagmus --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:nystagmus | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  301. en:ocular albinism type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ocular albinism type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  302. en:ocular albinism, type ii --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ocular albinism, type ii | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  303. en:oculo-dento-digital syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:oculo-dento-digital syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  304. en:oesophageal papilloma --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:oesophageal papilloma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  305. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  306. en:oligodactyly (45%) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:oligodactyly (45%) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  307. en:omphalocele --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:omphalocele | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  308. en:optic neuritis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:optic neuritis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  309. en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:orofaciodigital syndrome type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  310. en:orofaciodigital syndrome type 6 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:orofaciodigital syndrome type 6 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  311. en:osteochondrodysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:osteochondrodysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  312. en:otopalatodigital syndrome type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:otopalatodigital syndrome type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  313. en:pachyonychia congenita --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pachyonychia congenita | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  314. en:pancreatic lipase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pancreatic lipase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  315. en:pantothenate kinase-associated neurodegeneration --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pantothenate kinase-associated neurodegeneration | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  316. en:panuveitis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:panuveitis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  317. en:papillomatosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:papillomatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  318. en:parasitology --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:parasitology | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  319. en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:paroxysmal extreme pain disorder | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  320. en:partington x-linked mental retardation syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:partington x-linked mental retardation syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  321. en:pathological aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pathological aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  322. en:pearson marrow-pancreas syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pearson marrow-pancreas syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  323. en:pemphigoid gestationis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pemphigoid gestationis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  324. en:peritoneal panniculitis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:peritoneal panniculitis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  325. en:perthes disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:perthes disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  326. en:phakomatosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:phakomatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  327. en:pharmacotherapeutic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pharmacotherapeutic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  328. en:phosphoenolpyruvate carboxykinase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:phosphoenolpyruvate carboxykinase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  329. en:physiopathological --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:physiopathological | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  330. en:pinta --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pinta | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  331. en:piriformis muscle syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:piriformis muscle syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  332. en:pityriasis lichenoides --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pityriasis lichenoides | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  333. en:pityriasis rubra pilaris --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pityriasis rubra pilaris | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  334. en:plummer-vinson syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:plummer-vinson syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  335. en:poland syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:poland syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  336. en:polydactyly, postaxial --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:polydactyly, postaxial | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  337. en:porcn, 13-bp dup, nt1059 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porcn, 13-bp dup, nt1059 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  338. en:porcn, 178g-a, gly60arg --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porcn, 178g-a, gly60arg | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  339. en:porcn, arg365gln --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porcn, arg365gln | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  340. en:porcn, trp74ter --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porcn, trp74ter | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  341. en:porokeratosis, disseminated superficial actinic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porokeratosis, disseminated superficial actinic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  342. en:porphyria cutanea tarda --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:porphyria cutanea tarda | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  343. en:port wine stain --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:port wine stain | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  344. en:potocki-lupski syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:potocki-lupski syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  345. en:prekallikrein deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:prekallikrein deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  346. en:primary carnitine deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:primary carnitine deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  347. en:progressive bulbar palsy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:progressive bulbar palsy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  348. en:progressive muscular atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:progressive muscular atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  349. en:progressive supranuclear palsy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:progressive supranuclear palsy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  350. en:prosopagnosia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:prosopagnosia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  351. en:proteus-like syndrome (disorder) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:proteus-like syndrome (disorder) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  352. en:pseudotumor cerebri --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pseudotumor cerebri | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  353. en:pseudoxanthoma elasticum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pseudoxanthoma elasticum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  354. en:pterygium colli --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:pterygium colli | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  355. en:radiotherapeutic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:radiotherapeutic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  356. en:rare non-neoplastic disorder --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:rare non-neoplastic disorder | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  357. en:regional abnormality of skin --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:regional abnormality of skin | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  358. en:rehabilitation aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:rehabilitation aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  359. en:renpenning syndrome 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:renpenning syndrome 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  360. en:rett syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:rett syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  361. en:robinow syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:robinow syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  362. en:scimitar syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:scimitar syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  363. en:scleredema adultorum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:scleredema adultorum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  364. en:scoliosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:scoliosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  365. en:sea-blue histiocyte syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sea-blue histiocyte syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  366. en:seckel syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:seckel syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  367. en:selective antibody deficiency with normal immunoglobulins --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:selective antibody deficiency with normal immunoglobulins | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  368. en:senter syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:senter syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  369. en:septo-optic dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:septo-optic dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  370. en:short metatarsal bones --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:short metatarsal bones | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  371. en:short ribs --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:short ribs | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  372. en:short stature --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:short stature | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  373. en:short stature homeobox deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:short stature homeobox deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  374. en:shy-drager syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:shy-drager syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  375. en:simple syndactyly of fingers - first web --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:simple syndactyly of fingers - first web | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  376. en:simple syndactyly of fingers - second to fourth web --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:simple syndactyly of fingers - second to fourth web | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  377. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:simpson golabi behmel syndrome type 1 | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  378. en:sitosterolemia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sitosterolemia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  379. en:sjogren-larsson syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sjogren-larsson syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  380. en:skin atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:skin atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  381. en:skin diseases, genetic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:skin diseases, genetic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  382. en:skin neoplasm --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:skin neoplasm | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  383. en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:smith-lemli-opitz syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  384. en:sparse hair --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sparse hair | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  385. en:specified anomalies of nails --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:specified anomalies of nails | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  386. en:spheno-frontal dysostosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:spheno-frontal dysostosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  387. en:spinal muscular atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:spinal muscular atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  388. en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  389. en:spondyloepimetaphyseal dysplasia, sponastrime type --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:spondyloepimetaphyseal dysplasia, sponastrime type | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  390. en:spondyloepiphyseal dysplasia tarda, x-linked --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  391. en:stickler syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:stickler syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  392. en:stiff skin syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:stiff skin syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  393. en:subacute sclerosing panencephalitis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:subacute sclerosing panencephalitis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  394. en:sudden unexplained death in childhood --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sudden unexplained death in childhood | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  395. en:sudden unexplained infant death --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sudden unexplained infant death | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  396. en:surgical aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:surgical aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  397. en:sweet syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:sweet syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  398. en:swyer james syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:swyer james syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  399. en:syndactyly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:syndactyly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  400. en:syndactyly (75%) --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:syndactyly (75%) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  401. en:syndactyly of fingers --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:syndactyly of fingers | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  402. en:syndactyly of toes without bone fusion --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:syndactyly of toes without bone fusion | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  403. en:syringomyelia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:syringomyelia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  404. en:takotsubo cardiomyopathy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:takotsubo cardiomyopathy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  405. en:taxonomic --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:taxonomic | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  406. en:tay-sachs disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:tay-sachs disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  407. en:therapeutic aspects --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:therapeutic aspects | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  408. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:thiamin-responsive maple syrup urine disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  409. en:thoracic outlet syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:thoracic outlet syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  410. en:thyroid dysgenesis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:thyroid dysgenesis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  411. en:togaviridae infection --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:togaviridae infection | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  412. en:tooth and nail syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:tooth and nail syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  413. en:tracheobronchomegaly --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:tracheobronchomegaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  414. en:transient global amnesia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:transient global amnesia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  415. en:treacher collins syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:treacher collins syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  416. en:triploidy syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:triploidy syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  417. en:true hermaphroditism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:true hermaphroditism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  418. en:umbilical hernia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:umbilical hernia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  419. en:undescended testes --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:undescended testes | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  420. en:uniparental disomy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:uniparental disomy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  421. en:urticaria pigmentosa/maculopapular cutaneous mastocytosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:urticaria pigmentosa/maculopapular cutaneous mastocytosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  422. en:use of ultrasonography --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:use of ultrasonography | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  423. en:uveomeningoencephalitic syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:uveomeningoencephalitic syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  424. en:van der woude syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:van der woude syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  425. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  426. en:viruses --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:viruses | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  427. en:waisman syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:waisman syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  428. en:wallerian degeneration --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:wallerian degeneration | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  429. en:wandering spleen --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:wandering spleen | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  430. en:wegener granulomatosis --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:wegener granulomatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  431. en:whipple disease --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:whipple disease | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  432. en:x-linked adrenal hypoplasia congenita --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked adrenal hypoplasia congenita | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  433. en:x-linked bulbar-muscular atrophy --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked bulbar-muscular atrophy | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  434. en:x-linked creatine transporter deficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked creatine transporter deficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  435. en:x-linked dominant inheritance --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked dominant inheritance | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  436. en:x-linked dyskeratosis congenita --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked dyskeratosis congenita | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  437. en:x-linked dystonia parkinsonism --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked dystonia parkinsonism | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  438. en:x-linked hydrocephalus syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked hydrocephalus syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  439. en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  440. en:x-linked retinal dysplasia --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked retinal dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  441. en:x-linked severe combined immunodeficiency --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:x-linked severe combined immunodeficiency | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  442. en:xeroderma pigmentosum --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:xeroderma pigmentosum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  443. en:yellow nail syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=en:yellow nail syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  444. hypogonadisme avec anosmie --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=hypogonadisme avec anosmie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  445. hypoplasie --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=hypoplasie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  446. maladies --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=maladies | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  447. médecine --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=médecine | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  448. syndrome --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  449. syndrome d'hypoplasie dermique en aires --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=syndrome d'hypoplasie dermique en aires | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  450. syndrome de --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=syndrome de | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  451. syndrome de goltz-gorlin --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=syndrome de goltz-gorlin | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  452. tuberculose des méninges --- r_associated #0: 20 --> Goltz (syndrome de)
    n1=tuberculose des méninges | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  453. Haltia-Santavuori (maladie de) --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=Haltia-Santavuori (maladie de) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  454. Kallman --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=Kallman | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  455. déficit en céto-acide décarboxylase --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=déficit en céto-acide décarboxylase | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  456. goltz --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=goltz | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  457. hypophosphatasie --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=hypophosphatasie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  458. malformation d'Arnold-Chiari --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=malformation d'Arnold-Chiari | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  459. ptose splénique --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=ptose splénique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  460. rate ectopique --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=rate ectopique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  461. rate errante --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=rate errante | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  462. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=syndrome de Kallman-de Morsier | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  463. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> Goltz (syndrome de)
    n1=syndrome de de Morsier-Kallmann | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=15
  464. HELLP syndrome --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=HELLP syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  465. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  466. a-bêta-lipoprotéinémie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=a-bêta-lipoprotéinémie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  467. achromatopsie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=achromatopsie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  468. ainhum --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=ainhum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  469. albinisme --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=albinisme | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  470. aprosencéphalie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=aprosencéphalie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  471. aïnhum --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=aïnhum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  472. cataplexie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=cataplexie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  473. chondrodysplasia punctata --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=chondrodysplasia punctata | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  474. dentinogenesis imperfecta --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=dentinogenesis imperfecta | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  475. diabète bronzé --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=diabète bronzé | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  476. distichiasis --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=distichiasis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  477. dystrophie musculaire --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=dystrophie musculaire | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  478. dystrophie musculaire d'Emery-Dreifuss --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=dystrophie musculaire d'Emery-Dreifuss | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  479. déficience congénitale --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=déficience congénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  480. déformation congénitale --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=déformation congénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  481. en:Goltz syndrome --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=en:Goltz syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  482. en:Voorhœve syndrome --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=en:Voorhœve syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  483. en:tuberculosis of meninges (cerebral)(spinal) --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  484. erythromelalgia --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=erythromelalgia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  485. genu varum --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=genu varum | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  486. hamartoma --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=hamartoma | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  487. hamartome --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=hamartome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  488. hypophosphatasies --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=hypophosphatasies | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  489. hémochromatose primitive --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=hémochromatose primitive | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  490. leptoméningite tuberculeuse --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=leptoméningite tuberculeuse | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  491. leptospirose --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=leptospirose | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  492. lissencéphalie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=lissencéphalie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  493. maladie de Voorhoeve --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=maladie de Voorhoeve | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  494. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=maladie des urines à l'odeur de sirop d'érable | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  495. maladie du sirop d'érable --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=maladie du sirop d'érable | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  496. malocclusion --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=malocclusion | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  497. myéloméningocèle --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=myéloméningocèle | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  498. méningite tuberculeuse --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=méningite tuberculeuse | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  499. omphalocèle --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=omphalocèle | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  500. papillomatosis --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=papillomatosis | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  501. pinta --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=pinta | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  502. pterygium colli --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=pterygium colli | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  503. ptérygium colli --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=ptérygium colli | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  504. rate aberrante --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=rate aberrante | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  505. rate flottante --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=rate flottante | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  506. rate vagabonde --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=rate vagabonde | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  507. septo-optic dysplasia --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=septo-optic dysplasia | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  508. splénoptose --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=splénoptose | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  509. stiff skin syndrome --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=stiff skin syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  510. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  511. syndrome de Rathbun --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de Rathbun | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  512. syndrome de Rett --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de Rett | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  513. syndrome de Rokitansky --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de Rokitansky | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  514. syndrome de Rokitansky-Küster-Hauser --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de Rokitansky-Küster-Hauser | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  515. syndrome de de Morsier --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=syndrome de de Morsier | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  516. trachéo-bronchomégalie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=trachéo-bronchomégalie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  517. trachéobronchomégalie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=trachéobronchomégalie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  518. tuberculose méningée --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=tuberculose méningée | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  519. tumeur cutanée --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=tumeur cutanée | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  520. tumeur de la peau --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=tumeur de la peau | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  521. érythermalgie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=érythermalgie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  522. érythromélalgie --- r_associated #0: 10 --> Goltz (syndrome de)
    n1=érythromélalgie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=10
  523. abêtalipoprotéinémie --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=abêtalipoprotéinémie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  524. amnésie globale transitoire --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=amnésie globale transitoire | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  525. anomalie congénitale --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=anomalie congénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  526. atrophie cutanée --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=atrophie cutanée | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  527. atrophie de la peau --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=atrophie de la peau | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  528. atrophodermie --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=atrophodermie | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  529. coarctation aortique --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=coarctation aortique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  530. disomie uniparentale --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=disomie uniparentale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  531. en:Gray platelet syndrome --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=en:Gray platelet syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  532. en:Seckel syndrome --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=en:Seckel syndrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  533. en:congenital anomaly --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=en:congenital anomaly | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  534. examen non précisé, méningite tuberculeuse --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=examen non précisé, méningite tuberculeuse | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  535. hamartochondrome --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartochondrome | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  536. hamartomatose --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartomatose | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  537. hamartome achromique --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartome achromique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  538. hamartome achromique systématisé --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartome achromique systématisé | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  539. hamartome angio-eccrine --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartome angio-eccrine | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  540. hamartome anémique --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hamartome anémique | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  541. hémochromatose --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=hémochromatose | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  542. ichthyose congénitale --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=ichthyose congénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  543. maladie de Haltia-Santavuori --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=maladie de Haltia-Santavuori | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  544. maladie de Perthes --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=maladie de Perthes | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  545. maladie de Whipple --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=maladie de Whipple | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  546. maladie des urines avec odeur de sirop erable --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=maladie des urines avec odeur de sirop erable | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  547. malformation congénitale --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=malformation congénitale | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  548. myopathie primitive progressive --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=myopathie primitive progressive | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  549. ostéochondrodysplasies --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=ostéochondrodysplasies | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  550. syndrome de Goltz-Gorlin --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=syndrome de Goltz-Gorlin | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  551. syndrome de Jadassohn-Lewandowsky --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=syndrome de Jadassohn-Lewandowsky | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  552. syndrome de Stickler --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=syndrome de Stickler | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=5
  553. syndrome olfacto-génital --- r_associated #0: 5 --> Goltz (syndrome de)
    n1=syndrome olfacto-génital | n2=Goltz (syndrome de) | 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