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'en:combined molybdoflavoprotein enzyme deficiency'
(id=9095890 ; fe=en:combined molybdoflavoprotein enzyme deficiency ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1340 creation date=2017-10-27 touchdate=2025-03-23 09:02:34.000)
≈ 43 relations sortantes

  1. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 42 / 1 -> déficit en cofacteur molybdène
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=déficit en cofacteur molybdène | rel=r_associated | relid=0 | w=42
  2. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 38 / 0.905 -> déficit en xanthine-oxydase et en sulfite-oxydase
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=déficit en xanthine-oxydase et en sulfite-oxydase | rel=r_associated | relid=0 | w=38
  3. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 32 / 0.762 -> en:molybdenum cofactor deficiency
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=32
  4. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 31 / 0.738 -> déficit en enzyme molybdoflavoprotéique
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=déficit en enzyme molybdoflavoprotéique | rel=r_associated | relid=0 | w=31
  5. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 30 / 0.714 -> carence en cofacteur molybdène
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=carence en cofacteur molybdène | rel=r_associated | relid=0 | w=30
  6. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 30 / 0.714 -> xanthinurie héréditaire de type 2
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=xanthinurie héréditaire de type 2 | rel=r_associated | relid=0 | w=30
  7. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 25 / 0.595 -> en:combined
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:combined | rel=r_associated | relid=0 | w=25
  8. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 25 / 0.595 -> protéine
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=protéine | rel=r_associated | relid=0 | w=25
  9. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> coeur triatrial
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  10. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> déficit en molybdène-cofacteur
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=déficit en molybdène-cofacteur | rel=r_associated | relid=0 | w=20
  11. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:'ghost' peroxisomes in fibroblasts seen on immunofluorescence microscopy
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:'ghost' peroxisomes in fibroblasts seen on immunofluorescence microscopy | rel=r_associated | relid=0 | w=20
  12. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:abnormal isoelectric focusing of serum transferrin, type 2 pattern
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:abnormal isoelectric focusing of serum transferrin, type 2 pattern | rel=r_associated | relid=0 | w=20
  13. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:absence of protein-bound lipoic acid
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:absence of protein-bound lipoic acid | rel=r_associated | relid=0 | w=20
  14. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:acrodysostosis 1
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  15. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  16. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:carbonic anhydrase i deficiency
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  17. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:cor triatriatum
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  18. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  19. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:decreased activity of alpha-ketoglutarate dehydrogenase (alpha-kgdh)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:decreased activity of alpha-ketoglutarate dehydrogenase (alpha-kgdh) | rel=r_associated | relid=0 | w=20
  20. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:decreased activity of branched-chain ketoacid dehydrogenase (bckdh)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:decreased activity of branched-chain ketoacid dehydrogenase (bckdh) | rel=r_associated | relid=0 | w=20
  21. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:double stranded anti dna antibody
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:double stranded anti dna antibody | rel=r_associated | relid=0 | w=20
  22. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:eiken type chondrodysplasia
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  23. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:elevated liver enzymes during episodes
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:elevated liver enzymes during episodes | rel=r_associated | relid=0 | w=20
  24. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:elevated serum very long chain fatty acids (vlcfa)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:elevated serum very long chain fatty acids (vlcfa) | rel=r_associated | relid=0 | w=20
  25. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:hyperammonemia during episodes
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:hyperammonemia during episodes | rel=r_associated | relid=0 | w=20
  26. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased bilirubin (patient b)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased bilirubin (patient b) | rel=r_associated | relid=0 | w=20
  27. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased serum alpha-alanine (patient b)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased serum alpha-alanine (patient b) | rel=r_associated | relid=0 | w=20
  28. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased serum alpha-ketoglutarate
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased serum alpha-ketoglutarate | rel=r_associated | relid=0 | w=20
  29. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased serum glutamine (patient a)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased serum glutamine (patient a) | rel=r_associated | relid=0 | w=20
  30. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased serum insulin-like growth factor 1 {comment=hpo:probinson}
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased serum insulin-like growth factor 1 {comment=hpo:probinson} | rel=r_associated | relid=0 | w=20
  31. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased urinary glyoxylate (1 patient)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased urinary glyoxylate (1 patient) | rel=r_associated | relid=0 | w=20
  32. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:increased urinary s-(2-carboxypropyl)cysteine
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:increased urinary s-(2-carboxypropyl)cysteine | rel=r_associated | relid=0 | w=20
  33. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  34. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  35. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:mental retardation, autosomal dominant 9
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  36. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:mental retardation, autosomal recessive 34
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  37. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  38. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:mitochondrial dna depletion syndrome 12
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  39. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:molybdenum cofactor deficiency, complementation group a
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:molybdenum cofactor deficiency, complementation group a | rel=r_associated | relid=0 | w=20
  40. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:mucolipidosis type iii gamma
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  41. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:plasma kallikrein deficiency
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  42. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:secondarily decreased activity of the pyruvate dehydrogenase complex (pdc)
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:secondarily decreased activity of the pyruvate dehydrogenase complex (pdc) | rel=r_associated | relid=0 | w=20
  43. en:combined molybdoflavoprotein enzyme deficiency -- r_associated #0: 20 / 0.476 -> en:tissue kallikrein deficiency
    n1=en:combined molybdoflavoprotein enzyme deficiency | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
≈ 44 relations entrantes

  1. cœur triatrial --- r_associated #0: 50 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=cœur triatrial | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=50
  2. coeur triatrial --- r_associated #0: 46 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=coeur triatrial | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=46
  3. en:'ghost' peroxisomes in fibroblasts seen on immunofluorescence microscopy --- r_associated #0: 37 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:'ghost' peroxisomes in fibroblasts seen on immunofluorescence microscopy | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=37
  4. déficit en xanthine-oxydase et en sulfite-oxydase --- r_associated #0: 35 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=déficit en xanthine-oxydase et en sulfite-oxydase | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=35
  5. en:elevated serum very long chain fatty acids (vlcfa) --- r_associated #0: 35 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:elevated serum very long chain fatty acids (vlcfa) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=35
  6. déficit en enzyme molybdoflavoprotéique --- r_associated #0: 34 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=déficit en enzyme molybdoflavoprotéique | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=34
  7. en:carbonic anhydrase i deficiency --- r_associated #0: 34 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:carbonic anhydrase i deficiency | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=34
  8. en:eiken type chondrodysplasia --- r_associated #0: 34 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:eiken type chondrodysplasia | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=34
  9. en:increased urinary glyoxylate (1 patient) --- r_associated #0: 34 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased urinary glyoxylate (1 patient) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=34
  10. en:hyperammonemia during episodes --- r_associated #0: 32 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:hyperammonemia during episodes | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=32
  11. en:increased serum insulin-like growth factor 1 {comment=hpo:probinson} --- r_associated #0: 32 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased serum insulin-like growth factor 1 {comment=hpo:probinson} | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=32
  12. en:mental retardation, autosomal dominant 9 --- r_associated #0: 32 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:mental retardation, autosomal dominant 9 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=32
  13. en:mental retardation, autosomal recessive 34 --- r_associated #0: 32 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:mental retardation, autosomal recessive 34 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=32
  14. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 32 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=32
  15. en:increased serum alpha-alanine (patient b) --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased serum alpha-alanine (patient b) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  16. en:increased serum glutamine (patient a) --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased serum glutamine (patient a) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  17. en:increased urinary s-(2-carboxypropyl)cysteine --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased urinary s-(2-carboxypropyl)cysteine | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  18. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  19. en:secondarily decreased activity of the pyruvate dehydrogenase complex (pdc) --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:secondarily decreased activity of the pyruvate dehydrogenase complex (pdc) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  20. en:tissue kallikrein deficiency --- r_associated #0: 31 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:tissue kallikrein deficiency | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=31
  21. en:abnormal isoelectric focusing of serum transferrin, type 2 pattern --- r_associated #0: 30 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:abnormal isoelectric focusing of serum transferrin, type 2 pattern | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=30
  22. en:acrodysostosis 1 --- r_associated #0: 30 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:acrodysostosis 1 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=30
  23. en:decreased activity of alpha-ketoglutarate dehydrogenase (alpha-kgdh) --- r_associated #0: 30 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:decreased activity of alpha-ketoglutarate dehydrogenase (alpha-kgdh) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=30
  24. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 30 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=30
  25. carence en cofacteur molybdène --- r_associated #0: 29 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=carence en cofacteur molybdène | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=29
  26. en:elevated liver enzymes during episodes --- r_associated #0: 29 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:elevated liver enzymes during episodes | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=29
  27. en:increased bilirubin (patient b) --- r_associated #0: 29 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased bilirubin (patient b) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=29
  28. en:absence of protein-bound lipoic acid --- r_associated #0: 28 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:absence of protein-bound lipoic acid | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=28
  29. en:cor triatriatum --- r_associated #0: 28 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:cor triatriatum | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=28
  30. en:double stranded anti dna antibody --- r_associated #0: 28 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:double stranded anti dna antibody | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=28
  31. en:mucolipidosis type iii gamma --- r_associated #0: 28 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:mucolipidosis type iii gamma | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=28
  32. xanthinurie héréditaire de type 2 --- r_associated #0: 28 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=xanthinurie héréditaire de type 2 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=28
  33. déficit en cofacteur molybdène --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=déficit en cofacteur molybdène | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  34. déficit en molybdène-cofacteur --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=déficit en molybdène-cofacteur | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  35. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  36. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  37. en:increased serum alpha-ketoglutarate --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:increased serum alpha-ketoglutarate | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  38. en:molybdenum cofactor deficiency --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:molybdenum cofactor deficiency | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  39. en:molybdenum cofactor deficiency, complementation group a --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:molybdenum cofactor deficiency, complementation group a | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  40. en:plasma kallikrein deficiency --- r_associated #0: 27 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:plasma kallikrein deficiency | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=27
  41. en:decreased activity of branched-chain ketoacid dehydrogenase (bckdh) --- r_associated #0: 26 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:decreased activity of branched-chain ketoacid dehydrogenase (bckdh) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=26
  42. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 26 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=26
  43. déficit en immunoglobulines (syndrome de) --- r_associated #0: 10 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=déficit en immunoglobulines (syndrome de) | n2=en:combined molybdoflavoprotein enzyme deficiency | rel=r_associated | relid=0 | w=10
  44. molybdène-cofacteur (déficit en) --- r_associated #0: 5 --> en:combined molybdoflavoprotein enzyme deficiency
    n1=molybdène-cofacteur (déficit en) | n2=en:combined molybdoflavoprotein enzyme 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