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'en:complement component deficiency'
(id=6717063 ; fe=en:complement component deficiency ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1432 creation date=2017-06-21 touchdate=2025-10-09 18:30:29.000)
≈ 36 relations sortantes

  1. en:complement component deficiency -- r_associated #0: 35 / 1 -> en:congenital immunodeficiency involving the hematopoietic system
    n1=en:complement component deficiency | n2=en:congenital immunodeficiency involving the hematopoietic system | rel=r_associated | relid=0 | w=35
  2. en:complement component deficiency -- r_associated #0: 35 / 1 -> en:congenital neutropenia
    n1=en:complement component deficiency | n2=en:congenital neutropenia | rel=r_associated | relid=0 | w=35
  3. en:complement component deficiency -- r_associated #0: 35 / 1 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:complement component deficiency | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=35
  4. en:complement component deficiency -- r_associated #0: 35 / 1 -> en:x-linked agammaglobulinemia with growth hormone deficiency
    n1=en:complement component deficiency | n2=en:x-linked agammaglobulinemia with growth hormone deficiency | rel=r_associated | relid=0 | w=35
  5. en:complement component deficiency -- r_associated #0: 34 / 0.971 -> en:severe combined immunodeficiency
    n1=en:complement component deficiency | n2=en:severe combined immunodeficiency | rel=r_associated | relid=0 | w=34
  6. en:complement component deficiency -- r_associated #0: 32 / 0.914 -> en:ataxia telangiectasia syndrome
    n1=en:complement component deficiency | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=32
  7. en:complement component deficiency -- r_associated #0: 32 / 0.914 -> en:congenital hypergammaglobulinemia
    n1=en:complement component deficiency | n2=en:congenital hypergammaglobulinemia | rel=r_associated | relid=0 | w=32
  8. en:complement component deficiency -- r_associated #0: 32 / 0.914 -> en:hypopigmentation-immunodeficiency disease
    n1=en:complement component deficiency | n2=en:hypopigmentation-immunodeficiency disease | rel=r_associated | relid=0 | w=32
  9. en:complement component deficiency -- r_associated #0: 31 / 0.886 -> en:common variable immunodeficiency with predominant immunoregulatory t-cell disorders
    n1=en:complement component deficiency | n2=en:common variable immunodeficiency with predominant immunoregulatory t-cell disorders | rel=r_associated | relid=0 | w=31
  10. en:complement component deficiency -- r_associated #0: 30 / 0.857 -> en:bloom syndrome
    n1=en:complement component deficiency | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=30
  11. en:complement component deficiency -- r_associated #0: 30 / 0.857 -> en:chronic granulomatous disease
    n1=en:complement component deficiency | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=30
  12. en:complement component deficiency -- r_associated #0: 30 / 0.857 -> en:congenital
    n1=en:complement component deficiency | n2=en:congenital | rel=r_associated | relid=0 | w=30
  13. en:complement component deficiency -- r_associated #0: 30 / 0.857 -> en:nijmegen breakage syndrome
    n1=en:complement component deficiency | n2=en:nijmegen breakage syndrome | rel=r_associated | relid=0 | w=30
  14. en:complement component deficiency -- r_associated #0: 29 / 0.829 -> en:immune system finding
    n1=en:complement component deficiency | n2=en:immune system finding | rel=r_associated | relid=0 | w=29
  15. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:chediak-higashi syndrome
    n1=en:complement component deficiency | n2=en:chediak-higashi syndrome | rel=r_associated | relid=0 | w=28
  16. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:common variable immunodeficiency with predominant abnormalities of b-cell numbers and functions
    n1=en:complement component deficiency | n2=en:common variable immunodeficiency with predominant abnormalities of b-cell numbers and functions | rel=r_associated | relid=0 | w=28
  17. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:congenital agammaglobulinemia
    n1=en:complement component deficiency | n2=en:congenital agammaglobulinemia | rel=r_associated | relid=0 | w=28
  18. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:hereditary white blood cell disorder
    n1=en:complement component deficiency | n2=en:hereditary white blood cell disorder | rel=r_associated | relid=0 | w=28
  19. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:immunodeficiency with multicarboxylase deficiency
    n1=en:complement component deficiency | n2=en:immunodeficiency with multicarboxylase deficiency | rel=r_associated | relid=0 | w=28
  20. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:leukocyte adhesion deficiency
    n1=en:complement component deficiency | n2=en:leukocyte adhesion deficiency | rel=r_associated | relid=0 | w=28
  21. en:complement component deficiency -- r_associated #0: 28 / 0.8 -> en:thymic aplasia or dysplasia with immunodeficiency
    n1=en:complement component deficiency | n2=en:thymic aplasia or dysplasia with immunodeficiency | rel=r_associated | relid=0 | w=28
  22. en:complement component deficiency -- r_associated #0: 27 / 0.771 -> en:wiskott-aldrich syndrome
    n1=en:complement component deficiency | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=27
  23. en:complement component deficiency -- r_associated #0: 26 / 0.743 -> en:common variable immunodeficiency with autoantibodies to b- or t-cells
    n1=en:complement component deficiency | n2=en:common variable immunodeficiency with autoantibodies to b- or t-cells | rel=r_associated | relid=0 | w=26
  24. en:complement component deficiency -- r_associated #0: 26 / 0.743 -> en:hereditary angioedema
    n1=en:complement component deficiency | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=26
  25. en:complement component deficiency -- r_associated #0: 26 / 0.743 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:complement component deficiency | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=26
  26. en:complement component deficiency -- r_associated #0: 26 / 0.743 -> en:x-linked lymphoproliferative syndrome
    n1=en:complement component deficiency | n2=en:x-linked lymphoproliferative syndrome | rel=r_associated | relid=0 | w=26
  27. en:complement component deficiency -- r_associated #0: 25 / 0.714 -> en:complement
    n1=en:complement component deficiency | n2=en:complement | rel=r_associated | relid=0 | w=25
  28. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> congénital
    n1=en:complement component deficiency | n2=congénital | rel=r_associated | relid=0 | w=20
  29. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> congenital
    n1=en:complement component deficiency | n2=congenital | rel=r_associated | relid=0 | w=20
  30. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> congénitale
    n1=en:complement component deficiency | n2=congénitale | rel=r_associated | relid=0 | w=20
  31. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> contractures congénitales et arachnodactylie
    n1=en:complement component deficiency | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  32. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> déficit immunitaire combiné sévère
    n1=en:complement component deficiency | n2=déficit immunitaire combiné sévère | rel=r_associated | relid=0 | w=20
  33. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> en:immuno-osseous dysplasia
    n1=en:complement component deficiency | n2=en:immuno-osseous dysplasia | rel=r_associated | relid=0 | w=20
  34. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> en:Nezelof's syndrome
    n1=en:complement component deficiency | n2=en:Nezelof's syndrome | rel=r_associated | relid=0 | w=20
  35. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> nystagmus congénital isolé
    n1=en:complement component deficiency | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  36. en:complement component deficiency -- r_associated #0: 20 / 0.571 -> syndrome de Nezelof
    n1=en:complement component deficiency | n2=syndrome de Nezelof | rel=r_associated | relid=0 | w=20
≈ 50 relations entrantes

  1. en:congenital --- r_associated #0: 73 --> en:complement component deficiency
    n1=en:congenital | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=73
  2. congenital --- r_associated #0: 72 --> en:complement component deficiency
    n1=congenital | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=72
  3. congénitale --- r_associated #0: 61 --> en:complement component deficiency
    n1=congénitale | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=61
  4. congénital --- r_associated #0: 55 --> en:complement component deficiency
    n1=congénital | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=55
  5. en:common variable immunodeficiency with predominant immunoregulatory t-cell disorders --- r_associated #0: 43 --> en:complement component deficiency
    n1=en:common variable immunodeficiency with predominant immunoregulatory t-cell disorders | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=43
  6. déficit immunitaire combiné sévère --- r_associated #0: 42 --> en:complement component deficiency
    n1=déficit immunitaire combiné sévère | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=42
  7. en:severe combined immunodeficiency --- r_associated #0: 41 --> en:complement component deficiency
    n1=en:severe combined immunodeficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=41
  8. en:common variable immunodeficiency with predominant abnormalities of b-cell numbers and functions --- r_associated #0: 39 --> en:complement component deficiency
    n1=en:common variable immunodeficiency with predominant abnormalities of b-cell numbers and functions | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=39
  9. en:hereditary white blood cell disorder --- r_associated #0: 39 --> en:complement component deficiency
    n1=en:hereditary white blood cell disorder | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=39
  10. nystagmus congénital isolé --- r_associated #0: 38 --> en:complement component deficiency
    n1=nystagmus congénital isolé | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=38
  11. en:congenital agammaglobulinemia --- r_associated #0: 35 --> en:complement component deficiency
    n1=en:congenital agammaglobulinemia | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=35
  12. en:wiskott-aldrich syndrome --- r_associated #0: 34 --> en:complement component deficiency
    n1=en:wiskott-aldrich syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=34
  13. en:x-linked lymphoproliferative syndrome --- r_associated #0: 34 --> en:complement component deficiency
    n1=en:x-linked lymphoproliferative syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=34
  14. syndrome de Nezelof --- r_associated #0: 34 --> en:complement component deficiency
    n1=syndrome de Nezelof | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=34
  15. en:congenital neutropenia --- r_associated #0: 32 --> en:complement component deficiency
    n1=en:congenital neutropenia | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=32
  16. en:immune system finding --- r_associated #0: 31 --> en:complement component deficiency
    n1=en:immune system finding | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=31
  17. en:immunodeficiency with multicarboxylase deficiency --- r_associated #0: 30 --> en:complement component deficiency
    n1=en:immunodeficiency with multicarboxylase deficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=30
  18. en:hereditary angioedema --- r_associated #0: 29 --> en:complement component deficiency
    n1=en:hereditary angioedema | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=29
  19. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 29 --> en:complement component deficiency
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=29
  20. en:thymic aplasia or dysplasia with immunodeficiency --- r_associated #0: 29 --> en:complement component deficiency
    n1=en:thymic aplasia or dysplasia with immunodeficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=29
  21. en:x-linked agammaglobulinemia with growth hormone deficiency --- r_associated #0: 29 --> en:complement component deficiency
    n1=en:x-linked agammaglobulinemia with growth hormone deficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=29
  22. contractures congénitales et arachnodactylie --- r_associated #0: 28 --> en:complement component deficiency
    n1=contractures congénitales et arachnodactylie | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=28
  23. en:Nezelof's syndrome --- r_associated #0: 28 --> en:complement component deficiency
    n1=en:Nezelof's syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=28
  24. en:chronic granulomatous disease --- r_associated #0: 28 --> en:complement component deficiency
    n1=en:chronic granulomatous disease | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=28
  25. en:ataxia telangiectasia syndrome --- r_associated #0: 27 --> en:complement component deficiency
    n1=en:ataxia telangiectasia syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=27
  26. en:chediak-higashi syndrome --- r_associated #0: 27 --> en:complement component deficiency
    n1=en:chediak-higashi syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=27
  27. en:common variable immunodeficiency with autoantibodies to b- or t-cells --- r_associated #0: 27 --> en:complement component deficiency
    n1=en:common variable immunodeficiency with autoantibodies to b- or t-cells | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=27
  28. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 27 --> en:complement component deficiency
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=27
  29. en:immuno-osseous dysplasia --- r_associated #0: 27 --> en:complement component deficiency
    n1=en:immuno-osseous dysplasia | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=27
  30. en:leukocyte adhesion deficiency --- r_associated #0: 26 --> en:complement component deficiency
    n1=en:leukocyte adhesion deficiency | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=26
  31. en:congenital hypergammaglobulinemia --- r_associated #0: 25 --> en:complement component deficiency
    n1=en:congenital hypergammaglobulinemia | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=25
  32. en:congenital immunodeficiency involving the hematopoietic system --- r_associated #0: 25 --> en:complement component deficiency
    n1=en:congenital immunodeficiency involving the hematopoietic system | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=25
  33. en:hypopigmentation-immunodeficiency disease --- r_associated #0: 25 --> en:complement component deficiency
    n1=en:hypopigmentation-immunodeficiency disease | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=25
  34. en:nystagmus --- r_associated #0: 25 --> en:complement component deficiency
    n1=en:nystagmus | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=25
  35. en:bloom syndrome --- r_associated #0: 24 --> en:complement component deficiency
    n1=en:bloom syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=24
  36. adhérence leucocytaire (déficit d') --- r_associated #0: 23 --> en:complement component deficiency
    n1=adhérence leucocytaire (déficit d') | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=23
  37. agranulocytose constitutionnelle --- r_associated #0: 22 --> en:complement component deficiency
    n1=agranulocytose constitutionnelle | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=22
  38. en:nijmegen breakage syndrome --- r_associated #0: 22 --> en:complement component deficiency
    n1=en:nijmegen breakage syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=22
  39. immunodéficience combinée grave --- r_associated #0: 22 --> en:complement component deficiency
    n1=immunodéficience combinée grave | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=22
  40. CONGENITAL --- r_associated #0: 10 --> en:complement component deficiency
    n1=CONGENITAL | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  41. CONGÉNITALE --- r_associated #0: 10 --> en:complement component deficiency
    n1=CONGÉNITALE | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  42. Nezelof (syndrome de) --- r_associated #0: 10 --> en:complement component deficiency
    n1=Nezelof (syndrome de) | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  43. en:contractural arachnodactyly --- r_associated #0: 10 --> en:complement component deficiency
    n1=en:contractural arachnodactyly | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  44. nystagmus --- r_associated #0: 10 --> en:complement component deficiency
    n1=nystagmus | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  45. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:complement component deficiency
    n1=nystagmus héréditaire vertical | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  46. nystagmus lié au sexe --- r_associated #0: 10 --> en:complement component deficiency
    n1=nystagmus lié au sexe | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  47. nystagmus myoclonies --- r_associated #0: 10 --> en:complement component deficiency
    n1=nystagmus myoclonies | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  48. syndrome de Bridges et Good --- r_associated #0: 10 --> en:complement component deficiency
    n1=syndrome de Bridges et Good | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=10
  49. en:Nijmegen breakage syndrome --- r_associated #0: 5 --> en:complement component deficiency
    n1=en:Nijmegen breakage syndrome | n2=en:complement component deficiency | rel=r_associated | relid=0 | w=5
  50. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:complement component deficiency
    n1=nystagmus (zone de moindre) | n2=en:complement component deficiency | 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