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'en:leukokeratosis, hereditary mucosal'
(id=9102925 ; fe=en:leukokeratosis, hereditary mucosal ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2264 creation date=2017-10-29 touchdate=2025-03-23 09:02:34.000)
≈ 71 relations sortantes

  1. en:leukokeratosis, hereditary mucosal -- r_associated #0: 29 / 1 -> kératose héréditaire des muqueuses
    n1=en:leukokeratosis, hereditary mucosal | n2=kératose héréditaire des muqueuses | rel=r_associated | relid=0 | w=29
  2. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:17q11.2 microduplication syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
  3. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:absence of fingerprints with congenital milia syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20
  4. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:acro-dermato-ungual-lacrimal-tooth syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20
  5. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:acrodysostosis 1
    n1=en:leukokeratosis, hereditary mucosal | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  6. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:leukokeratosis, hereditary mucosal | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  7. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:aniridia and intellectual disability syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  8. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20
  9. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
    n1=en:leukokeratosis, hereditary mucosal | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20
  10. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:aphalangy and syndactyly with microcephaly syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
  11. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:leukokeratosis, hereditary mucosal | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  12. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:autosomal dominant beta2-microglobulinic amyloidosis
    n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=20
  13. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20
  14. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:autosomal dominant charcot-marie-tooth disease type 2m
    n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=20
  15. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:autosomal dominant focal dystonia dyt25 type
    n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
  16. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia
    n1=en:leukokeratosis, hereditary mucosal | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20
  17. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:bamforth syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  18. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:bethlem myopathy 1
    n1=en:leukokeratosis, hereditary mucosal | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=20
  19. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20
  20. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cannon's disease
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cannon's disease | rel=r_associated | relid=0 | w=20
  21. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:carbonic anhydrase i deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  22. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cardiac anomaly and heterotaxy syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  23. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cataract glaucoma syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20
  24. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:chronic diarrhea with villous atrophy syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:chronic diarrhea with villous atrophy syndrome | rel=r_associated | relid=0 | w=20
  25. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cleidorhizomelic syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20
  26. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cor triatriatum
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  27. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:corneal dystrophy, subepithelial mucinous
    n1=en:leukokeratosis, hereditary mucosal | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20
  28. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  29. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  30. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  31. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:czech dysplasia, metatarsal type
    n1=en:leukokeratosis, hereditary mucosal | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20
  32. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  33. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20
  34. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20
  35. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:ehlers-danlos syndrome vascular-like type
    n1=en:leukokeratosis, hereditary mucosal | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20
  36. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:eiken type chondrodysplasia
    n1=en:leukokeratosis, hereditary mucosal | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  37. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:epiphyseal dysplasia, multiple, 2
    n1=en:leukokeratosis, hereditary mucosal | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20
  38. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:familial median cleft of upper and lower lip
    n1=en:leukokeratosis, hereditary mucosal | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  39. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:gracile bone dysplasia
    n1=en:leukokeratosis, hereditary mucosal | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20
  40. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:halal syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  41. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
  42. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hereditary sensory and autonomic neuropathy type 1b
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=20
  43. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hyperinsulinism due to hnf1a deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=20
  44. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hyperinsulinism due to insulin receptor deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=20
  45. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  46. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:hyperuricemia, anemia, renal failure syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=20
  47. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
    n1=en:leukokeratosis, hereditary mucosal | n2=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | rel=r_associated | relid=0 | w=20
  48. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  49. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  50. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:mental retardation, autosomal dominant 9
    n1=en:leukokeratosis, hereditary mucosal | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  51. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:mental retardation, autosomal recessive 34
    n1=en:leukokeratosis, hereditary mucosal | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  52. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  53. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:leukokeratosis, hereditary mucosal | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  54. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:mitochondrial dna depletion syndrome 12
    n1=en:leukokeratosis, hereditary mucosal | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  55. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:morava mehes syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20
  56. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:moyamoya disease with early onset achalasia
    n1=en:leukokeratosis, hereditary mucosal | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  57. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:mucolipidosis type iii gamma
    n1=en:leukokeratosis, hereditary mucosal | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  58. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:piussan lenaerts mathieu syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  59. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:plasma kallikrein deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  60. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:polydactyly, preaxial ii (disorder)
    n1=en:leukokeratosis, hereditary mucosal | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=20
  61. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:preaxial deficiency, postaxial polydactyly and hypospadias
    n1=en:leukokeratosis, hereditary mucosal | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20
  62. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:primary pigmented nodular adrenocortical disease
    n1=en:leukokeratosis, hereditary mucosal | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=20
  63. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | rel=r_associated | relid=0 | w=20
  64. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:short fifth metacarpal insulin resistance syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20
  65. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:spinocerebellar ataxia type 32
    n1=en:leukokeratosis, hereditary mucosal | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=20
  66. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:spinocerebellar ataxia type 37
    n1=en:leukokeratosis, hereditary mucosal | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=20
  67. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:steatocystoma multiplex with natal tooth syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:steatocystoma multiplex with natal tooth syndrome | rel=r_associated | relid=0 | w=20
  68. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:timothy syndrome type 2
    n1=en:leukokeratosis, hereditary mucosal | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20
  69. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:tissue kallikrein deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  70. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:tubular renal disease with cardiomyopathy syndrome
    n1=en:leukokeratosis, hereditary mucosal | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20
  71. en:leukokeratosis, hereditary mucosal -- r_associated #0: 20 / 0.69 -> en:white sponge nevus 1
    n1=en:leukokeratosis, hereditary mucosal | n2=en:white sponge nevus 1 | rel=r_associated | relid=0 | w=20
≈ 74 relations entrantes

  1. cœur triatrial --- r_associated #0: 50 --> en:leukokeratosis, hereditary mucosal
    n1=cœur triatrial | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=50
  2. coeur triatrial --- r_associated #0: 49 --> en:leukokeratosis, hereditary mucosal
    n1=coeur triatrial | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=49
  3. en:aniridia and intellectual disability syndrome --- r_associated #0: 40 --> en:leukokeratosis, hereditary mucosal
    n1=en:aniridia and intellectual disability syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=40
  4. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 40 --> en:leukokeratosis, hereditary mucosal
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=40
  5. en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 39 --> en:leukokeratosis, hereditary mucosal
    n1=en:corneal dystrophy, subepithelial mucinous | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=39
  6. en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  7. en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  8. en:cannon's disease --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:cannon's disease | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  9. en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  10. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  11. en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  12. en:piussan lenaerts mathieu syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:piussan lenaerts mathieu syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  13. en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 35 --> en:leukokeratosis, hereditary mucosal
    n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=35
  14. en:acrodysostosis 1 --- r_associated #0: 34 --> en:leukokeratosis, hereditary mucosal
    n1=en:acrodysostosis 1 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=34
  15. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 34 --> en:leukokeratosis, hereditary mucosal
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=34
  16. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 34 --> en:leukokeratosis, hereditary mucosal
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=34
  17. en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 34 --> en:leukokeratosis, hereditary mucosal
    n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=34
  18. en:spinocerebellar ataxia type 37 --- r_associated #0: 34 --> en:leukokeratosis, hereditary mucosal
    n1=en:spinocerebellar ataxia type 37 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=34
  19. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  20. en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  21. en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  22. en:bamforth syndrome --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:bamforth syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  23. en:bethlem myopathy 1 --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:bethlem myopathy 1 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  24. en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  25. en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  26. en:mental retardation, autosomal dominant 9 --- r_associated #0: 32 --> en:leukokeratosis, hereditary mucosal
    n1=en:mental retardation, autosomal dominant 9 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  27. en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  28. en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  29. en:cataract glaucoma syndrome --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:cataract glaucoma syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  30. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  31. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  32. en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  33. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  34. en:spinocerebellar ataxia type 32 --- r_associated #0: 31 --> en:leukokeratosis, hereditary mucosal
    n1=en:spinocerebellar ataxia type 32 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31
  35. en:carbonic anhydrase i deficiency --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:carbonic anhydrase i deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  36. en:czech dysplasia, metatarsal type --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:czech dysplasia, metatarsal type | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  37. en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:ehlers-danlos syndrome vascular-like type | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  38. en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  39. en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  40. en:plasma kallikrein deficiency --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:plasma kallikrein deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  41. en:timothy syndrome type 2 --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=en:timothy syndrome type 2 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  42. kératose héréditaire des muqueuses --- r_associated #0: 30 --> en:leukokeratosis, hereditary mucosal
    n1=kératose héréditaire des muqueuses | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=30
  43. en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 29 --> en:leukokeratosis, hereditary mucosal
    n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=29
  44. en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 29 --> en:leukokeratosis, hereditary mucosal
    n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=29
  45. en:gracile bone dysplasia --- r_associated #0: 29 --> en:leukokeratosis, hereditary mucosal
    n1=en:gracile bone dysplasia | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=29
  46. en:tissue kallikrein deficiency --- r_associated #0: 29 --> en:leukokeratosis, hereditary mucosal
    n1=en:tissue kallikrein deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=29
  47. en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 29 --> en:leukokeratosis, hereditary mucosal
    n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=29
  48. en:17q11.2 microduplication syndrome --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:17q11.2 microduplication syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  49. en:chronic diarrhea with villous atrophy syndrome --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:chronic diarrhea with villous atrophy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  50. en:cor triatriatum --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:cor triatriatum | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  51. en:familial median cleft of upper and lower lip --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:familial median cleft of upper and lower lip | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  52. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  53. en:mucolipidosis type iii gamma --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:mucolipidosis type iii gamma | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  54. en:white sponge nevus 1 --- r_associated #0: 28 --> en:leukokeratosis, hereditary mucosal
    n1=en:white sponge nevus 1 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=28
  55. en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:absence of fingerprints with congenital milia syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  56. en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  57. en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  58. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  59. en:morava mehes syndrome --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:morava mehes syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  60. en:moyamoya disease with early onset achalasia --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:moyamoya disease with early onset achalasia | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  61. en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome --- r_associated #0: 27 --> en:leukokeratosis, hereditary mucosal
    n1=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=27
  62. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  63. en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  64. en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  65. en:cleidorhizomelic syndrome --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:cleidorhizomelic syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  66. en:eiken type chondrodysplasia --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:eiken type chondrodysplasia | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  67. en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  68. en:halal syndrome --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:halal syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  69. en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  70. en:mental retardation, autosomal recessive 34 --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:mental retardation, autosomal recessive 34 | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  71. en:polydactyly, preaxial ii (disorder) --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:polydactyly, preaxial ii (disorder) | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  72. en:primary pigmented nodular adrenocortical disease --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:primary pigmented nodular adrenocortical disease | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  73. en:steatocystoma multiplex with natal tooth syndrome --- r_associated #0: 26 --> en:leukokeratosis, hereditary mucosal
    n1=en:steatocystoma multiplex with natal tooth syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=26
  74. absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:leukokeratosis, hereditary mucosal
    n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=10
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