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'en:alport syndrome, x-linked'
(id=8563174 ; fe=en:alport syndrome, x-linked ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2000 creation date=2017-08-01 touchdate=2025-07-24 21:46:13.000)
≈ 51 relations sortantes

  1. en:alport syndrome, x-linked -- r_associated #0: 41 / 1 -> en:col4a5, gly521cys
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly521cys | rel=r_associated | relid=0 | w=41
  2. en:alport syndrome, x-linked -- r_associated #0: 41 / 1 -> en:x-linked dominant inheritance
    n1=en:alport syndrome, x-linked | n2=en:x-linked dominant inheritance | rel=r_associated | relid=0 | w=41
  3. en:alport syndrome, x-linked -- r_associated #0: 38 / 0.927 -> en:col4a5, 3-prime and partial 5-prime deletion
    n1=en:alport syndrome, x-linked | n2=en:col4a5, 3-prime and partial 5-prime deletion | rel=r_associated | relid=0 | w=38
  4. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:alport syndrome
    n1=en:alport syndrome, x-linked | n2=en:alport syndrome | rel=r_associated | relid=0 | w=35
  5. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:col4a5, cys108ser
    n1=en:alport syndrome, x-linked | n2=en:col4a5, cys108ser | rel=r_associated | relid=0 | w=35
  6. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:col4a5, gly1143asp
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly1143asp | rel=r_associated | relid=0 | w=35
  7. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:col4a5, gly289val and arg1421cys
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly289val and arg1421cys | rel=r_associated | relid=0 | w=35
  8. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:col4a5, gly325glu
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly325glu | rel=r_associated | relid=0 | w=35
  9. en:alport syndrome, x-linked -- r_associated #0: 35 / 0.854 -> en:hereditary nephritis
    n1=en:alport syndrome, x-linked | n2=en:hereditary nephritis | rel=r_associated | relid=0 | w=35
  10. en:alport syndrome, x-linked -- r_associated #0: 34 / 0.829 -> en:alport syndrome, autosomal dominant
    n1=en:alport syndrome, x-linked | n2=en:alport syndrome, autosomal dominant | rel=r_associated | relid=0 | w=34
  11. en:alport syndrome, x-linked -- r_associated #0: 34 / 0.829 -> en:col4a5 wt allele
    n1=en:alport syndrome, x-linked | n2=en:col4a5 wt allele | rel=r_associated | relid=0 | w=34
  12. en:alport syndrome, x-linked -- r_associated #0: 34 / 0.829 -> en:col4a5, gly54asp
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly54asp | rel=r_associated | relid=0 | w=34
  13. en:alport syndrome, x-linked -- r_associated #0: 34 / 0.829 -> en:col4a5, trp1538ser
    n1=en:alport syndrome, x-linked | n2=en:col4a5, trp1538ser | rel=r_associated | relid=0 | w=34
  14. en:alport syndrome, x-linked -- r_associated #0: 32 / 0.78 -> en:col4a5 gene
    n1=en:alport syndrome, x-linked | n2=en:col4a5 gene | rel=r_associated | relid=0 | w=32
  15. en:alport syndrome, x-linked -- r_associated #0: 32 / 0.78 -> en:col4a5, gly325arg
    n1=en:alport syndrome, x-linked | n2=en:col4a5, gly325arg | rel=r_associated | relid=0 | w=32
  16. en:alport syndrome, x-linked -- r_associated #0: 32 / 0.78 -> syndrome d'Alport
    n1=en:alport syndrome, x-linked | n2=syndrome d'Alport | rel=r_associated | relid=0 | w=32
  17. en:alport syndrome, x-linked -- r_associated #0: 31 / 0.756 -> en:col4a5, 10-15-kb ins, 40-kb del
    n1=en:alport syndrome, x-linked | n2=en:col4a5, 10-15-kb ins, 40-kb del | rel=r_associated | relid=0 | w=31
  18. en:alport syndrome, x-linked -- r_associated #0: 31 / 0.756 -> en:col4a5, 38-kb del
    n1=en:alport syndrome, x-linked | n2=en:col4a5, 38-kb del | rel=r_associated | relid=0 | w=31
  19. en:alport syndrome, x-linked -- r_associated #0: 30 / 0.732 -> en:alport syndrome, autosomal recessive
    n1=en:alport syndrome, x-linked | n2=en:alport syndrome, autosomal recessive | rel=r_associated | relid=0 | w=30
  20. en:alport syndrome, x-linked -- r_associated #0: 28 / 0.683 -> en:col4a5, 450-kb del
    n1=en:alport syndrome, x-linked | n2=en:col4a5, 450-kb del | rel=r_associated | relid=0 | w=28
  21. en:alport syndrome, x-linked -- r_associated #0: 28 / 0.683 -> en:col4a5, leu1649arg
    n1=en:alport syndrome, x-linked | n2=en:col4a5, leu1649arg | rel=r_associated | relid=0 | w=28
  22. en:alport syndrome, x-linked -- r_associated #0: 27 / 0.659 -> en:col4a5, arg1677gln
    n1=en:alport syndrome, x-linked | n2=en:col4a5, arg1677gln | rel=r_associated | relid=0 | w=27
  23. en:alport syndrome, x-linked -- r_associated #0: 27 / 0.659 -> en:corneal erosion
    n1=en:alport syndrome, x-linked | n2=en:corneal erosion | rel=r_associated | relid=0 | w=27
  24. en:alport syndrome, x-linked -- r_associated #0: 26 / 0.634 -> en:col4a5, ex5-10del
    n1=en:alport syndrome, x-linked | n2=en:col4a5, ex5-10del | rel=r_associated | relid=0 | w=26
  25. en:alport syndrome, x-linked -- r_associated #0: 25 / 0.61 -> syndrome
    n1=en:alport syndrome, x-linked | n2=syndrome | rel=r_associated | relid=0 | w=25
  26. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:chitayat meunier hodgkinson syndrome
    n1=en:alport syndrome, x-linked | n2=en:chitayat meunier hodgkinson syndrome | rel=r_associated | relid=0 | w=20
  27. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:chromosome xp22.3 microdeletion syndrome
    n1=en:alport syndrome, x-linked | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  28. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:chronic renal failure
    n1=en:alport syndrome, x-linked | n2=en:chronic renal failure | rel=r_associated | relid=0 | w=20
  29. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:congenital disorder of glycosylation type 1s
    n1=en:alport syndrome, x-linked | n2=en:congenital disorder of glycosylation type 1s | rel=r_associated | relid=0 | w=20
  30. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:Diskinson's syndrome
    n1=en:alport syndrome, x-linked | n2=en:Diskinson's syndrome | rel=r_associated | relid=0 | w=20
  31. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:alport syndrome, x-linked | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20
  32. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:female carriers may show intermittent hematuria
    n1=en:alport syndrome, x-linked | n2=en:female carriers may show intermittent hematuria | rel=r_associated | relid=0 | w=20
  33. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:fried syndrome
    n1=en:alport syndrome, x-linked | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20
  34. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:hearing loss occurs in late childhood
    n1=en:alport syndrome, x-linked | n2=en:hearing loss occurs in late childhood | rel=r_associated | relid=0 | w=20
  35. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
    n1=en:alport syndrome, x-linked | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
  36. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:primary ciliary dyskinesia and retinitis pigmentosa syndrome
    n1=en:alport syndrome, x-linked | n2=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20
  37. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:scholte syndrome
    n1=en:alport syndrome, x-linked | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  38. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability armfield type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
  39. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability cantagrel type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20
  40. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability miles carpenter type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=20
  41. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability pai type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20
  42. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability seemanova type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
  43. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability stevenson type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
  44. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability stoll type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
  45. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability van esch type
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20
  46. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  47. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability with ataxia and apraxia syndrome
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
  48. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  49. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
    n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=20
  50. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> insuffisance rénale chronique
    n1=en:alport syndrome, x-linked | n2=insuffisance rénale chronique | rel=r_associated | relid=0 | w=20
  51. en:alport syndrome, x-linked -- r_associated #0: 20 / 0.488 -> syndrome d'alport
    n1=en:alport syndrome, x-linked | n2=syndrome d'alport | rel=r_associated | relid=0 | w=20
≈ 56 relations entrantes

  1. syndrome d'Alport --- r_associated #0: 167 --> en:alport syndrome, x-linked
    n1=syndrome d'Alport | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=167
  2. en:Diskinson's syndrome --- r_associated #0: 165 --> en:alport syndrome, x-linked
    n1=en:Diskinson's syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=165
  3. syndrome d'alport --- r_associated #0: 54 --> en:alport syndrome, x-linked
    n1=syndrome d'alport | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=54
  4. en:alport syndrome --- r_associated #0: 46 --> en:alport syndrome, x-linked
    n1=en:alport syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=46
  5. en:col4a5, gly54asp --- r_associated #0: 43 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly54asp | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=43
  6. en:x-linked intellectual disability armfield type --- r_associated #0: 43 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability armfield type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=43
  7. en:alport syndrome, autosomal recessive --- r_associated #0: 41 --> en:alport syndrome, x-linked
    n1=en:alport syndrome, autosomal recessive | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=41
  8. en:col4a5, leu1649arg --- r_associated #0: 41 --> en:alport syndrome, x-linked
    n1=en:col4a5, leu1649arg | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=41
  9. en:congenital disorder of glycosylation type 1s --- r_associated #0: 40 --> en:alport syndrome, x-linked
    n1=en:congenital disorder of glycosylation type 1s | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=40
  10. en:chronic renal failure --- r_associated #0: 39 --> en:alport syndrome, x-linked
    n1=en:chronic renal failure | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=39
  11. insuffisance rénale chronique --- r_associated #0: 39 --> en:alport syndrome, x-linked
    n1=insuffisance rénale chronique | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=39
  12. en:col4a5, 450-kb del --- r_associated #0: 36 --> en:alport syndrome, x-linked
    n1=en:col4a5, 450-kb del | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=36
  13. en:corneal erosion --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:corneal erosion | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  14. en:female carriers may show intermittent hematuria --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:female carriers may show intermittent hematuria | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  15. en:fried syndrome --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:fried syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  16. en:hearing loss occurs in late childhood --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:hearing loss occurs in late childhood | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  17. en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  18. en:x-linked intellectual disability van esch type --- r_associated #0: 35 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability van esch type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=35
  19. en:col4a5, cys108ser --- r_associated #0: 34 --> en:alport syndrome, x-linked
    n1=en:col4a5, cys108ser | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=34
  20. en:col4a5, gly289val and arg1421cys --- r_associated #0: 34 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly289val and arg1421cys | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=34
  21. en:x-linked intellectual disability seemanova type --- r_associated #0: 34 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability seemanova type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=34
  22. en:x-linked intellectual disability stoll type --- r_associated #0: 34 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability stoll type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=34
  23. en:col4a5, gly325arg --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly325arg | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  24. en:col4a5, gly521cys --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly521cys | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  25. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  26. en:primary ciliary dyskinesia and retinitis pigmentosa syndrome --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  27. en:scholte syndrome --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:scholte syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  28. en:x-linked intellectual disability stevenson type --- r_associated #0: 32 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability stevenson type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=32
  29. en:col4a5, gly1143asp --- r_associated #0: 31 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly1143asp | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=31
  30. en:x-linked intellectual disability miles carpenter type --- r_associated #0: 31 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability miles carpenter type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=31
  31. défaillance rénale chronique --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=défaillance rénale chronique | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  32. en:chitayat meunier hodgkinson syndrome --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:chitayat meunier hodgkinson syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  33. en:chronic kidney insufficiency --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:chronic kidney insufficiency | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  34. en:col4a5, trp1538ser --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:col4a5, trp1538ser | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  35. en:x-linked intellectual disability cantagrel type --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability cantagrel type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  36. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  37. en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  38. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 30 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30
  39. en:chromosome xp22.3 microdeletion syndrome --- r_associated #0: 29 --> en:alport syndrome, x-linked
    n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=29
  40. en:col4a5, arg1677gln --- r_associated #0: 28 --> en:alport syndrome, x-linked
    n1=en:col4a5, arg1677gln | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=28
  41. en:x-linked intellectual disability pai type --- r_associated #0: 28 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability pai type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=28
  42. en:alport syndrome, autosomal dominant --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:alport syndrome, autosomal dominant | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  43. en:col4a5 wt allele --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:col4a5 wt allele | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  44. en:col4a5, 3-prime and partial 5-prime deletion --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:col4a5, 3-prime and partial 5-prime deletion | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  45. en:col4a5, 38-kb del --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:col4a5, 38-kb del | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  46. en:col4a5, ex5-10del --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:col4a5, ex5-10del | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  47. en:col4a5, gly325glu --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:col4a5, gly325glu | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  48. en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome --- r_associated #0: 27 --> en:alport syndrome, x-linked
    n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=27
  49. IRC
    (médecine)
     --- r_associated #0: 26 --> en:alport syndrome, x-linked
    n1=IRC
    (médecine)
    | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=26
  50. en:col4a5, 10-15-kb ins, 40-kb del --- r_associated #0: 26 --> en:alport syndrome, x-linked
    n1=en:col4a5, 10-15-kb ins, 40-kb del | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=26
  51. en:col4a5 gene --- r_associated #0: 20 --> en:alport syndrome, x-linked
    n1=en:col4a5 gene | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=20
  52. en:hereditary nephritis --- r_associated #0: 20 --> en:alport syndrome, x-linked
    n1=en:hereditary nephritis | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=20
  53. en:x-linked dominant inheritance --- r_associated #0: 20 --> en:alport syndrome, x-linked
    n1=en:x-linked dominant inheritance | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=20
  54. IRC --- r_associated #0: 10 --> en:alport syndrome, x-linked
    n1=IRC | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=10
  55. insuffisance respiratoire chronique --- r_associated #0: 5 --> en:alport syndrome, x-linked
    n1=insuffisance respiratoire chronique | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=5
  56. insuffisance rénale (neuropathie et) --- r_associated #0: 5 --> en:alport syndrome, x-linked
    n1=insuffisance rénale (neuropathie et) | n2=en:alport syndrome, x-linked | 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