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'en:hereditary sensory autonomic neuropathy, type 5'
(id=9103487 ; fe=en:hereditary sensory autonomic neuropathy, type 5 ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1072 creation date=2017-10-29 touchdate=2025-11-05 17:33:55.000)
≈ 33 relations sortantes

  1. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 36 / 1 -> neuropathie héréditaire sensorielle et autonome de type 5
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=neuropathie héréditaire sensorielle et autonome de type 5 | rel=r_associated | relid=0 | w=36
  2. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 32 / 0.889 -> neuropathie héréditaire sensitive et autonome de type v
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=neuropathie héréditaire sensitive et autonome de type v | rel=r_associated | relid=0 | w=32
  3. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 28 / 0.778 -> neuropathie héréditaire sensitive et autonome de type 5
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=neuropathie héréditaire sensitive et autonome de type 5 | rel=r_associated | relid=0 | w=28
  4. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 27 / 0.75 -> neuropathie héréditaire sensorielle et autonome de type v
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=neuropathie héréditaire sensorielle et autonome de type v | rel=r_associated | relid=0 | w=27
  5. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 26 / 0.722 -> en:congenital pain insensitivity
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=26
  6. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 26 / 0.722 -> neuropathie
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=neuropathie | rel=r_associated | relid=0 | w=26
  7. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 25 / 0.694 -> en:hereditary
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:hereditary | rel=r_associated | relid=0 | w=25
  8. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> coeur triatrial
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  9. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:acrodysostosis 1
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  10. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  11. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:carbonic anhydrase i deficiency
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  12. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:congenital analbuminemia
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  13. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:congenital cyst of aryepiglottic fold
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:congenital cyst of aryepiglottic fold | rel=r_associated | relid=0 | w=20
  14. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:congenital laryngeal cyst
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:congenital laryngeal cyst | rel=r_associated | relid=0 | w=20
  15. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:congenital megaprepuce
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:congenital megaprepuce | rel=r_associated | relid=0 | w=20
  16. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:cor triatriatum
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  17. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  18. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:eiken type chondrodysplasia
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  19. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:indifference to pain, congenital, autosomal recessive
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:indifference to pain, congenital, autosomal recessive | rel=r_associated | relid=0 | w=20
  20. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:infantile onset
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:infantile onset | rel=r_associated | relid=0 | w=20
  21. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  22. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  23. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:mental retardation, autosomal dominant 9
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  24. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:mental retardation, autosomal recessive 34
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  25. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  26. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:mitochondrial dna depletion syndrome 12
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  27. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:mucolipidosis type iii gamma
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  28. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:ngf, 680c-a and 2-bp del, 681gg
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:ngf, 680c-a and 2-bp del, 681gg | rel=r_associated | relid=0 | w=20
  29. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:ngf, arg211trp
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:ngf, arg211trp | rel=r_associated | relid=0 | w=20
  30. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:pigmented paravenous chorioretinal atrophy
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
  31. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:plasma kallikrein deficiency
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  32. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> en:tissue kallikrein deficiency
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  33. en:hereditary sensory autonomic neuropathy, type 5 -- r_associated #0: 20 / 0.556 -> rétinite pigmentaire paraveineuse
    n1=en:hereditary sensory autonomic neuropathy, type 5 | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
≈ 36 relations entrantes

  1. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 39 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=39
  2. neuropathie héréditaire sensitive et autonome de type v --- r_associated #0: 37 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=neuropathie héréditaire sensitive et autonome de type v | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=37
  3. en:carbonic anhydrase i deficiency --- r_associated #0: 35 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:carbonic anhydrase i deficiency | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=35
  4. en:congenital cyst of aryepiglottic fold --- r_associated #0: 35 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:congenital cyst of aryepiglottic fold | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=35
  5. en:indifference to pain, congenital, autosomal recessive --- r_associated #0: 35 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:indifference to pain, congenital, autosomal recessive | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=35
  6. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 35 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=35
  7. neuropathie héréditaire sensorielle et autonome de type v --- r_associated #0: 35 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=neuropathie héréditaire sensorielle et autonome de type v | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=35
  8. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 34 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=34
  9. en:mental retardation, autosomal dominant 9 --- r_associated #0: 34 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:mental retardation, autosomal dominant 9 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=34
  10. en:plasma kallikrein deficiency --- r_associated #0: 34 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:plasma kallikrein deficiency | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=34
  11. en:congenital pain insensitivity --- r_associated #0: 32 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:congenital pain insensitivity | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=32
  12. en:ngf, 680c-a and 2-bp del, 681gg --- r_associated #0: 32 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:ngf, 680c-a and 2-bp del, 681gg | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=32
  13. en:pigmented paravenous chorioretinal atrophy --- r_associated #0: 32 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=32
  14. rétinite pigmentaire paraveineuse --- r_associated #0: 32 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=rétinite pigmentaire paraveineuse | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=32
  15. en:acrodysostosis 1 --- r_associated #0: 31 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:acrodysostosis 1 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=31
  16. en:mucolipidosis type iii gamma --- r_associated #0: 31 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:mucolipidosis type iii gamma | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=31
  17. cœur triatrial --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=cœur triatrial | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  18. coeur triatrial --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=coeur triatrial | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  19. en:congenital megaprepuce --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:congenital megaprepuce | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  20. en:cor triatriatum --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:cor triatriatum | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  21. en:eiken type chondrodysplasia --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:eiken type chondrodysplasia | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  22. neuropathie héréditaire sensorielle et autonome de type 5 --- r_associated #0: 30 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=neuropathie héréditaire sensorielle et autonome de type 5 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=30
  23. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 29 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=29
  24. neuropathie héréditaire sensitive et autonome de type 5 --- r_associated #0: 29 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=neuropathie héréditaire sensitive et autonome de type 5 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=29
  25. en:mental retardation, autosomal recessive 34 --- r_associated #0: 28 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:mental retardation, autosomal recessive 34 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=28
  26. en:tissue kallikrein deficiency --- r_associated #0: 28 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:tissue kallikrein deficiency | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=28
  27. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 27 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=27
  28. en:infantile onset --- r_associated #0: 27 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:infantile onset | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=27
  29. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 27 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=27
  30. en:ngf, arg211trp --- r_associated #0: 27 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:ngf, arg211trp | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=27
  31. en:congenital analbuminemia --- r_associated #0: 26 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:congenital analbuminemia | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=26
  32. en:congenital laryngeal cyst --- r_associated #0: 26 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:congenital laryngeal cyst | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=26
  33. neuropathie --- r_associated #0: 20 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=neuropathie | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=20
  34. Neuropathie --- r_associated #0: 10 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=Neuropathie | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=10
  35. en:neuropathy --- r_associated #0: 10 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=en:neuropathy | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=10
  36. rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> en:hereditary sensory autonomic neuropathy, type 5
    n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:hereditary sensory autonomic neuropathy, type 5 | rel=r_associated | relid=0 | w=10
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