Javascript doit fonctionner ! Activez-le et rechargez cette page.
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)
 

'en:acatalasia'
(id=9966033 ; fe=en:acatalasia ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1261 creation date=2018-02-20 touchdate=2025-11-02 07:58:42.000)
≈ 40 relations sortantes

  1. en:acatalasia -- r_associated #0: 49 / 1 -> acatalasémie
    n1=en:acatalasia | n2=acatalasémie | rel=r_associated | relid=0 | w=49
  2. en:acatalasia -- r_associated #0: 48 / 0.98 -> en:acatalasemia
    n1=en:acatalasia | n2=en:acatalasemia | rel=r_associated | relid=0 | w=48
  3. en:acatalasia -- r_associated #0: 44 / 0.898 -> maladie de Takahara
    n1=en:acatalasia | n2=maladie de Takahara | rel=r_associated | relid=0 | w=44
  4. en:acatalasia -- r_associated #0: 42 / 0.857 -> acatalasies
    n1=en:acatalasia | n2=acatalasies | rel=r_associated | relid=0 | w=42
  5. en:acatalasia -- r_associated #0: 30 / 0.612 -> acatalasémie de type japonais
    n1=en:acatalasia | n2=acatalasémie de type japonais | rel=r_associated | relid=0 | w=30
  6. en:acatalasia -- r_associated #0: 30 / 0.612 -> acatalasie
    n1=en:acatalasia | n2=acatalasie | rel=r_associated | relid=0 | w=30
  7. en:acatalasia -- r_associated #0: 29 / 0.592 -> acatalasémie de type suisse
    n1=en:acatalasia | n2=acatalasémie de type suisse | rel=r_associated | relid=0 | w=29
  8. en:acatalasia -- r_associated #0: 29 / 0.592 -> catalase
    n1=en:acatalasia | n2=catalase | rel=r_associated | relid=0 | w=29
  9. en:acatalasia -- r_associated #0: 27 / 0.551 -> déficience en catalase
    n1=en:acatalasia | n2=déficience en catalase | rel=r_associated | relid=0 | w=27
  10. en:acatalasia -- r_associated #0: 27 / 0.551 -> déficit en catalase
    n1=en:acatalasia | n2=déficit en catalase | rel=r_associated | relid=0 | w=27
  11. en:acatalasia -- r_associated #0: 27 / 0.551 -> maladie de takahara
    n1=en:acatalasia | n2=maladie de takahara | rel=r_associated | relid=0 | w=27
  12. en:acatalasia -- r_associated #0: 26 / 0.531 -> en:catalase deficiency
    n1=en:acatalasia | n2=en:catalase deficiency | rel=r_associated | relid=0 | w=26
  13. en:acatalasia -- r_associated #0: 23 / 0.469 -> en:acatalasemia japanese type
    n1=en:acatalasia | n2=en:acatalasemia japanese type | rel=r_associated | relid=0 | w=23
  14. en:acatalasia -- r_associated #0: 23 / 0.469 -> processus pathologique
    n1=en:acatalasia | n2=processus pathologique | rel=r_associated | relid=0 | w=23
  15. en:acatalasia -- r_associated #0: 22 / 0.449 -> acatalasique
    n1=en:acatalasia | n2=acatalasique | rel=r_associated | relid=0 | w=22
  16. en:acatalasia -- r_associated #0: 22 / 0.449 -> en:acatalasemia swiss type
    n1=en:acatalasia | n2=en:acatalasemia swiss type | rel=r_associated | relid=0 | w=22
  17. en:acatalasia -- r_associated #0: 22 / 0.449 -> en:hypocatalasemia
    n1=en:acatalasia | n2=en:hypocatalasemia | rel=r_associated | relid=0 | w=22
  18. en:acatalasia -- r_associated #0: 20 / 0.408 -> coeur triatrial
    n1=en:acatalasia | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  19. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:acrodysostosis 1
    n1=en:acatalasia | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  20. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:alders syndrome
    n1=en:acatalasia | n2=en:alders syndrome | rel=r_associated | relid=0 | w=20
  21. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:acatalasia | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  22. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:carbonic anhydrase i deficiency
    n1=en:acatalasia | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  23. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:cor triatriatum
    n1=en:acatalasia | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  24. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:acatalasia | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  25. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia
    n1=en:acatalasia | n2=en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia | rel=r_associated | relid=0 | w=20
  26. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:eiken type chondrodysplasia
    n1=en:acatalasia | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  27. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:isolated alkyldihydroxyacetone phosphate synthase deficiency
    n1=en:acatalasia | n2=en:isolated alkyldihydroxyacetone phosphate synthase deficiency | rel=r_associated | relid=0 | w=20
  28. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:isolated dihydroxyacetone phosphate acyltransferase deficiency
    n1=en:acatalasia | n2=en:isolated dihydroxyacetone phosphate acyltransferase deficiency | rel=r_associated | relid=0 | w=20
  29. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:acatalasia | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  30. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:acatalasia | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  31. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:mental retardation, autosomal dominant 9
    n1=en:acatalasia | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  32. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:mental retardation, autosomal recessive 34
    n1=en:acatalasia | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  33. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:acatalasia | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  34. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:mitochondrial dna depletion syndrome 12
    n1=en:acatalasia | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  35. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:mucolipidosis type iii gamma
    n1=en:acatalasia | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  36. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:other group 2 peroxisomal disorders
    n1=en:acatalasia | n2=en:other group 2 peroxisomal disorders | rel=r_associated | relid=0 | w=20
  37. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:plasma kallikrein deficiency
    n1=en:acatalasia | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  38. en:acatalasia -- r_associated #0: 20 / 0.408 -> en:tissue kallikrein deficiency
    n1=en:acatalasia | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  39. en:acatalasia -- r_associated #0: 15 / 0.306 -> en:Takahara's disease
    n1=en:acatalasia | n2=en:Takahara's disease | rel=r_associated | relid=0 | w=15
  40. en:acatalasia -- r_associated #0: 15 / 0.306 -> Takahara (maladie de)
    n1=en:acatalasia | n2=Takahara (maladie de) | rel=r_associated | relid=0 | w=15
≈ 38 relations entrantes

  1. maladie de takahara --- r_associated #0: 48 --> en:acatalasia
    n1=maladie de takahara | n2=en:acatalasia | rel=r_associated | relid=0 | w=48
  2. maladie de Takahara --- r_associated #0: 45 --> en:acatalasia
    n1=maladie de Takahara | n2=en:acatalasia | rel=r_associated | relid=0 | w=45
  3. acatalasémie --- r_associated #0: 43 --> en:acatalasia
    n1=acatalasémie | n2=en:acatalasia | rel=r_associated | relid=0 | w=43
  4. en:Takahara's disease --- r_associated #0: 42 --> en:acatalasia
    n1=en:Takahara's disease | n2=en:acatalasia | rel=r_associated | relid=0 | w=42
  5. en:carbonic anhydrase i deficiency --- r_associated #0: 42 --> en:acatalasia
    n1=en:carbonic anhydrase i deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=42
  6. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 41 --> en:acatalasia
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=41
  7. Takahara (maladie de) --- r_associated #0: 40 --> en:acatalasia
    n1=Takahara (maladie de) | n2=en:acatalasia | rel=r_associated | relid=0 | w=40
  8. en:plasma kallikrein deficiency --- r_associated #0: 40 --> en:acatalasia
    n1=en:plasma kallikrein deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=40
  9. en:acatalasemia --- r_associated #0: 39 --> en:acatalasia
    n1=en:acatalasemia | n2=en:acatalasia | rel=r_associated | relid=0 | w=39
  10. en:other group 2 peroxisomal disorders --- r_associated #0: 35 --> en:acatalasia
    n1=en:other group 2 peroxisomal disorders | n2=en:acatalasia | rel=r_associated | relid=0 | w=35
  11. acatalasies --- r_associated #0: 34 --> en:acatalasia
    n1=acatalasies | n2=en:acatalasia | rel=r_associated | relid=0 | w=34
  12. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 34 --> en:acatalasia
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=34
  13. en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia --- r_associated #0: 32 --> en:acatalasia
    n1=en:dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia | n2=en:acatalasia | rel=r_associated | relid=0 | w=32
  14. en:mucolipidosis type iii gamma --- r_associated #0: 32 --> en:acatalasia
    n1=en:mucolipidosis type iii gamma | n2=en:acatalasia | rel=r_associated | relid=0 | w=32
  15. en:alders syndrome --- r_associated #0: 31 --> en:acatalasia
    n1=en:alders syndrome | n2=en:acatalasia | rel=r_associated | relid=0 | w=31
  16. cœur triatrial --- r_associated #0: 30 --> en:acatalasia
    n1=cœur triatrial | n2=en:acatalasia | rel=r_associated | relid=0 | w=30
  17. coeur triatrial --- r_associated #0: 30 --> en:acatalasia
    n1=coeur triatrial | n2=en:acatalasia | rel=r_associated | relid=0 | w=30
  18. en:mental retardation, autosomal recessive 34 --- r_associated #0: 29 --> en:acatalasia
    n1=en:mental retardation, autosomal recessive 34 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
  19. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 29 --> en:acatalasia
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
  20. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 29 --> en:acatalasia
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
  21. en:tissue kallikrein deficiency --- r_associated #0: 29 --> en:acatalasia
    n1=en:tissue kallikrein deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=29
  22. en:eiken type chondrodysplasia --- r_associated #0: 28 --> en:acatalasia
    n1=en:eiken type chondrodysplasia | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
  23. en:isolated alkyldihydroxyacetone phosphate synthase deficiency --- r_associated #0: 28 --> en:acatalasia
    n1=en:isolated alkyldihydroxyacetone phosphate synthase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
  24. en:isolated dihydroxyacetone phosphate acyltransferase deficiency --- r_associated #0: 28 --> en:acatalasia
    n1=en:isolated dihydroxyacetone phosphate acyltransferase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
  25. en:mental retardation, autosomal dominant 9 --- r_associated #0: 28 --> en:acatalasia
    n1=en:mental retardation, autosomal dominant 9 | n2=en:acatalasia | rel=r_associated | relid=0 | w=28
  26. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 27 --> en:acatalasia
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=27
  27. acatalasie --- r_associated #0: 26 --> en:acatalasia
    n1=acatalasie | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
  28. en:acrodysostosis 1 --- r_associated #0: 26 --> en:acatalasia
    n1=en:acrodysostosis 1 | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
  29. en:cor triatriatum --- r_associated #0: 26 --> en:acatalasia
    n1=en:cor triatriatum | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
  30. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 26 --> en:acatalasia
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=26
  31. acatalasémie de type japonais --- r_associated #0: 21 --> en:acatalasia
    n1=acatalasémie de type japonais | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
  32. acatalasémie de type suisse --- r_associated #0: 21 --> en:acatalasia
    n1=acatalasémie de type suisse | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
  33. déficience en catalase --- r_associated #0: 21 --> en:acatalasia
    n1=déficience en catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
  34. déficit en catalase --- r_associated #0: 21 --> en:acatalasia
    n1=déficit en catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=21
  35. catalase --- r_associated #0: 20 --> en:acatalasia
    n1=catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=20
  36. en:catalase deficiency --- r_associated #0: 20 --> en:acatalasia
    n1=en:catalase deficiency | n2=en:acatalasia | rel=r_associated | relid=0 | w=20
  37. Catalase --- r_associated #0: 10 --> en:acatalasia
    n1=Catalase | n2=en:acatalasia | rel=r_associated | relid=0 | w=10
  38. en:catalase --- r_associated #0: 10 --> en:acatalasia
    n1=en:catalase | n2=en:acatalasia | 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